U.S. flag

An official website of the United States government

nsv5515285

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,351

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
Submitted genomic14,539,136-14,542,486Question Mark
Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):14,649,948-14,653,298Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5515285Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1914,539,13614,542,486
nsv5515285RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1914,649,94814,653,298

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721707deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721707Submitted genomicNC_000019.10:g.145
39136_14542486del
GRCh38 (hg38)NC_000019.10Chr1914,539,13614,542,486
nssv17721707RemappedPerfectNC_000019.9:g.1464
9948_14653298del
GRCh37.p13First PassNC_000019.9Chr1914,649,94814,653,298

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)
nssv17721707<0.00136404
Support Center