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nsv898369

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:485,117

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1738 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):107,087,578-107,572,694Question Mark
Overlapping variant regions from other studies: 1738 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):106,958,304-107,443,420Question Mark
Overlapping variant regions from other studies: 757 SVs from 26 studies. See in: genome view    
Submitted genomic106,463,514-106,948,630Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv898369RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11107,087,578107,100,755107,568,531107,572,694
nsv898369RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11106,958,304106,971,481107,439,257107,443,420
nsv898369Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr11106,463,514106,476,691106,944,467106,948,630

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1579212copy number gainIS35053SNP arraySNP genotyping analysis10
nssv1595110copy number gainIS40111SNP arraySNP genotyping analysis12

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1579212RemappedPerfectNC_000011.10:g.(10
7087578_107100755)
_(107568531_107572
694)dup		GRCh38.p12First PassNC_000011.10Chr11107,087,578107,100,755107,568,531107,572,694
nssv1595110RemappedPerfectNC_000011.10:g.(10
7087578_107100755)
_(107568531_107572
694)dup		GRCh38.p12First PassNC_000011.10Chr11107,087,578107,100,755107,568,531107,572,694
nssv1579212RemappedPerfectNC_000011.9:g.(106
958304_106971481)_
(107439257_1074434
20)dup		GRCh37.p13First PassNC_000011.9Chr11106,958,304106,971,481107,439,257107,443,420
nssv1595110RemappedPerfectNC_000011.9:g.(106
958304_106971481)_
(107439257_1074434
20)dup		GRCh37.p13First PassNC_000011.9Chr11106,958,304106,971,481107,439,257107,443,420
nssv1579212Submitted genomicNC_000011.8:g.(106
463514_106476691)_
(106944467_1069486
30)dup		NCBI36 (hg18)NC_000011.8Chr11106,463,514106,476,691106,944,467106,948,630
nssv1595110Submitted genomicNC_000011.8:g.(106
463514_106476691)_
(106944467_1069486
30)dup		NCBI36 (hg18)NC_000011.8Chr11106,463,514106,476,691106,944,467106,948,630

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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