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nsv5466434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,736

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
Submitted genomic52,526,849-52,528,584Question Mark
Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):52,391,647-52,393,382Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5466434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr652,526,84952,528,584
nsv5466434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr652,391,64752,393,382

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16982807deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16982807Submitted genomicNC_000006.12:g.525
26849_52528584del
GRCh38 (hg38)NC_000006.12Chr652,526,84952,528,584
nssv16982807RemappedPerfectNC_000006.11:g.523
91647_52393382del
GRCh37.p13First PassNC_000006.11Chr652,391,64752,393,382

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)
nssv16982807<0.00126404
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