U.S. flag

An official website of the United States government

nsv5522569

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:121

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 21 studies. See in: genome view    
Submitted genomic68,581,447-68,581,567Question Mark
Overlapping variant regions from other studies: 107 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):66,577,588-66,577,708Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522569Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1768,581,44768,581,567
nsv5522569RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1766,577,58866,577,708

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714229deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714229Submitted genomicNC_000017.11:g.685
81447_68581567del
GRCh38 (hg38)NC_000017.11Chr1768,581,44768,581,567
nssv17714229RemappedPerfectNC_000017.10:g.665
77588_66577708del
GRCh37.p13First PassNC_000017.10Chr1766,577,58866,577,708

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)
nssv17714229<0.00126404
Support Center