U.S. flag

An official website of the United States government

nsv6147277

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,971

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 166 SVs from 46 studies. See in: genome view    
Submitted genomic29,459,290-29,465,260Question Mark
Overlapping variant regions from other studies: 166 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):29,950,197-29,956,167Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147277Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1929,459,29029,465,260
nsv6147277RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1929,950,19729,956,167

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722652mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722652Submitted genomicNC_000019.10:g.294
59290_29465260del
GRCh38 (hg38)NC_000019.10Chr1929,459,29029,465,260
nssv17722652RemappedPerfectNC_000019.9:g.2995
0197_29956167del
GRCh37.p13First PassNC_000019.9Chr1929,950,19729,956,167

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)
nssv177226520.51633046404
Support Center