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nsv5498341

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,062

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 27 studies. See in: genome view    
Submitted genomic66,652,296-66,656,357Question Mark
Overlapping variant regions from other studies: 97 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):66,419,767-66,423,828Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5498341Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1166,652,29666,656,357
nsv5498341RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,419,76766,423,828

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046215deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046215Submitted genomicNC_000011.10:g.666
52296_66656357del
GRCh38 (hg38)NC_000011.10Chr1166,652,29666,656,357
nssv17046215RemappedPerfectNC_000011.9:g.6641
9767_66423828del
GRCh37.p13First PassNC_000011.9Chr1166,419,76766,423,828

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)
nssv17046215<0.00126404
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