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nsv1338872

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:798,202

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2777 SVs from 101 studies. See in: genome view    
Remapped(Score: Pass):61,578,038-62,376,239Question Mark
Overlapping variant regions from other studies: 1134 SVs from 85 studies. See in: genome view    
Remapped(Score: Pass):62,180,400-62,294,432Question Mark
Overlapping variant regions from other studies: 1973 SVs from 94 studies. See in: genome view    
Remapped(Score: Pass):62,303,646-62,510,065Question Mark
Overlapping variant regions from other studies: 36 SVs from 14 studies. See in: genome view    
Remapped(Score: Pass):331,112-610,898Question Mark
Overlapping variant regions from other studies: 2548 SVs from 98 studies. See in: genome view    
Remapped(Score: Perfect):61,747,897-61,970,443Question Mark
Overlapping variant regions from other studies: 919 SVs from 27 studies. See in: genome view    
Submitted genomic61,385,332-61,607,878Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1338872RemappedPassGRCh38.p12Primary AssemblySecond PassNC_000007.14Chr761,578,03862,376,239
nsv1338872RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr762,180,40062,294,432
nsv1338872RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr762,303,64662,510,065
nsv1338872RemappedPassGRCh38.p12Primary AssemblySecond PassNT_187383.1Chr16|NT_1
87383.1		331,112610,898
nsv1338872RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr761,747,89761,970,443
nsv1338872Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr761,385,33261,607,878

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv8341641copy number lossSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv8341641RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNC_000007.1
4:g.(?_62303646)_(
62510065_?)delNT_1
87383.1:g.(?_33111
2)_(610898_?)delNC
_000007.14:g.(?_62
180400)_(62294432_
?)del		GRCh38.p12Second PassNC_000007.14Chr761,578,03862,376,239
nssv8341641RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNC_000007.1
4:g.(?_62303646)_(
62510065_?)delNT_1
87383.1:g.(?_33111
2)_(610898_?)delNC
_000007.14:g.(?_62
180400)_(62294432_
?)del		GRCh38.p12First PassNC_000007.14Chr762,180,40062,294,432
nssv8341641RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNC_000007.1
4:g.(?_62303646)_(
62510065_?)delNT_1
87383.1:g.(?_33111
2)_(610898_?)delNC
_000007.14:g.(?_62
180400)_(62294432_
?)del		GRCh38.p12First PassNC_000007.14Chr762,303,64662,510,065
nssv8341641RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)delNC_000007.1
4:g.(?_62303646)_(
62510065_?)delNT_1
87383.1:g.(?_33111
2)_(610898_?)delNC
_000007.14:g.(?_62
180400)_(62294432_
?)del		GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1		331,112610,898
nssv8341641RemappedPerfectNC_000007.13:g.(?_
61747897)_(6197044
3_?)del		GRCh37.p13First PassNC_000007.13Chr761,747,89761,970,443
nssv8341641Submitted genomicNC_000007.12:g.(?_
61385332)_(6160787
8_?)del		NCBI36 (hg18)NC_000007.12Chr761,385,33261,607,878

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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