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nsv5525265

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:84

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 27 studies. See in: genome view    
Submitted genomic67,788,245-67,788,328Question Mark
Overlapping variant regions from other studies: 116 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):67,822,148-67,822,231Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525265Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1667,788,24567,788,328
nsv5525265RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1667,822,14867,822,231

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707527deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707527Submitted genomicNC_000016.10:g.677
88245_67788328del
GRCh38 (hg38)NC_000016.10Chr1667,788,24567,788,328
nssv17707527RemappedPerfectNC_000016.9:g.6782
2148_67822231del
GRCh37.p13First PassNC_000016.9Chr1667,822,14867,822,231

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)
nssv17707527<0.00116404
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