U.S. flag

An official website of the United States government

nsv4224991

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:500,792

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 329 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):36,693,507-37,194,298Question Mark
Overlapping variant regions from other studies: 329 SVs from 20 studies. See in: genome view    
Submitted genomic37,267,644-37,768,435Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4224991RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1336,693,50737,194,298
nsv4224991Submitted genomicGRCh37.p13Primary AssemblyNC_000013.10Chr1337,267,64437,768,435

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15816201deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15816201RemappedPerfectNC_000013.11:g.366
93507_37194298del
GRCh38.p12First PassNC_000013.11Chr1336,693,50737,194,298
nssv15816201Submitted genomicNC_000013.10:g.372
67644_37768435del
GRCh37.p13NC_000013.10Chr1337,267,64437,768,435

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)
nssv158162014.6e-005121694
Support Center