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nsv5529671

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:251

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 149 SVs from 32 studies. See in: genome view    
Submitted genomic88,855,496-88,855,746Question Mark
Overlapping variant regions from other studies: 149 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):89,398,727-89,398,977Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529671Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1588,855,49688,855,746
nsv5529671RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1589,398,72789,398,977

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704082deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704082Submitted genomicNC_000015.10:g.888
55496_88855746del
GRCh38 (hg38)NC_000015.10Chr1588,855,49688,855,746
nssv17704082RemappedPerfectNC_000015.9:g.8939
8727_89398977del
GRCh37.p13First PassNC_000015.9Chr1589,398,72789,398,977

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)
nssv17704082<0.00126404
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