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nsv5421295

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,510

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 170 SVs from 30 studies. See in: genome view    
Submitted genomic177,982,661-177,988,170Question Mark
Overlapping variant regions from other studies: 172 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):177,951,796-177,957,305Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5421295Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1177,982,661177,988,170
nsv5421295RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1177,951,796177,957,305

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892638duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892638Submitted genomicNC_000001.11:g.177
982661_177988170du
p
GRCh38 (hg38)NC_000001.11Chr1177,982,661177,988,170
nssv16892638RemappedPerfectNC_000001.10:g.177
951796_177957305du
p
GRCh37.p13First PassNC_000001.10Chr1177,951,796177,957,305

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)
nssv16892638<0.00116404
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