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nsv896324

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:176,535

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2382 SVs from 107 studies. See in: genome view    
Remapped(Score: Perfect):133,412,162-133,588,696Question Mark
Overlapping variant regions from other studies: 2382 SVs from 107 studies. See in: genome view    
Remapped(Score: Perfect):135,225,666-135,402,200Question Mark
Overlapping variant regions from other studies: 995 SVs from 33 studies. See in: genome view    
Submitted genomic135,075,656-135,252,190Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv896324RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nsv896324RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nsv896324Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1521969copy number gainSP52680SNP arraySNP genotyping analysis9
nssv1531459copy number gainMS10445SNP arraySNP genotyping analysis11
nssv1536779copy number gainMS12947SNP arraySNP genotyping analysis22
nssv1536945copy number gainMS13028SNP arraySNP genotyping analysis13
nssv1539700copy number gainMS14451SNP arraySNP genotyping analysis9
nssv1540181copy number gainMS14724SNP arraySNP genotyping analysis15
nssv1541486copy number gainMS15337SNP arraySNP genotyping analysis10
nssv1541875copy number gainMS15515SNP arraySNP genotyping analysis13
nssv1545511copy number gainMS16821SNP arraySNP genotyping analysis11
nssv1547798copy number gainMS17562SNP arraySNP genotyping analysis12
nssv1551148copy number gainMS18799SNP arraySNP genotyping analysis9
nssv1555174copy number gainMS21216SNP arraySNP genotyping analysis12
nssv1558153copy number gainMS23142SNP arraySNP genotyping analysis10
nssv1562454copy number gainMS25589SNP arraySNP genotyping analysis13
nssv1567413copy number gainIS31074SNP arraySNP genotyping analysis39
nssv1570071copy number gainIS31778SNP arraySNP genotyping analysis13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1521969RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1531459RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1536779RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1536945RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1539700RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1540181RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1541486RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1541875RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1545511RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1547798RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1551148RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1555174RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1558153RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1562454RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1567413RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1570071RemappedPerfectNC_000010.11:g.(13
3412162_133432340)
_(133572278_133588
696)dup
GRCh38.p12First PassNC_000010.11Chr10133,412,162133,432,340133,572,278133,588,696
nssv1521969RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1531459RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1536779RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1536945RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1539700RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1540181RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1541486RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1541875RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1545511RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1547798RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1551148RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1555174RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1558153RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1562454RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1567413RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1570071RemappedPerfectNC_000010.10:g.(13
5225666_135245844)
_(135385782_135402
200)dup
GRCh37.p13First PassNC_000010.10Chr10135,225,666135,245,844135,385,782135,402,200
nssv1521969Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1531459Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1536779Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1536945Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1539700Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1540181Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1541486Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1541875Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1545511Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1547798Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1551148Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1555174Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1558153Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1562454Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1567413Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190
nssv1570071Submitted genomicNC_000010.9:g.(135
075656_135095834)_
(135235772_1352521
90)dup
NCBI36 (hg18)NC_000010.9Chr10135,075,656135,095,834135,235,772135,252,190

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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