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nsv5624213

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 24 studies. See in: genome view    
Submitted genomic94,043,620-94,043,620Question Mark
Overlapping variant regions from other studies: 111 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):93,762,464-93,762,464Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5624213Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr394,043,62094,043,620
nsv5624213RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr393,762,46493,762,464

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17120992insertionSAMN00001229SequencingSequence alignment1,149

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17120992Submitted genomicNC_000003.12:g.940
43620_94043621ins8
00
GRCh38 (hg38)NC_000003.12Chr394,043,62094,043,620
nssv17120992RemappedPerfectNC_000003.11:g.937
62464_93762465ins8
00
GRCh37.p13First PassNC_000003.11Chr393,762,46493,762,464

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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