U.S. flag

An official website of the United States government

nsv5526575

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:141

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 15 studies. See in: genome view    
Submitted genomic78,173,173-78,173,313Question Mark
Overlapping variant regions from other studies: 125 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):76,169,254-76,169,394Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526575Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1778,173,17378,173,313
nsv5526575RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1776,169,25476,169,394

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714834deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714834Submitted genomicNC_000017.11:g.781
73173_78173313del
GRCh38 (hg38)NC_000017.11Chr1778,173,17378,173,313
nssv17714834RemappedPerfectNC_000017.10:g.761
69254_76169394del
GRCh37.p13First PassNC_000017.10Chr1776,169,25476,169,394

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)
nssv17714834<0.00116404
Support Center