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nsv6142454

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:147,401

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 311 SVs from 48 studies. See in: genome view    
Submitted genomic40,284,000-40,431,400Question Mark
Overlapping variant regions from other studies: 540 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):42,429,018-42,576,418Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6142454Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr940,284,00040,431,400
nsv6142454RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr942,429,01842,576,418

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17022515duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17022515Submitted genomicNC_000009.12:g.402
84000_40431400dup
GRCh38 (hg38)NC_000009.12Chr940,284,00040,431,400
nssv17022515RemappedPerfectNC_000009.11:g.424
29018_42576418dup
GRCh37.p13First PassNC_000009.11Chr942,429,01842,576,418

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv170225150.0381042716
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