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nsv5417773

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 30 studies. See in: genome view    
Submitted genomic167,913,656-167,913,730Question Mark
Overlapping variant regions from other studies: 142 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):167,882,894-167,882,968Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5417773Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1167,913,656167,913,730
nsv5417773RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1167,882,894167,882,968

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892097deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892097Submitted genomicNC_000001.11:g.167
913656_167913730de
l
GRCh38 (hg38)NC_000001.11Chr1167,913,656167,913,730
nssv16892097RemappedPerfectNC_000001.10:g.167
882894_167882968de
l
GRCh37.p13First PassNC_000001.10Chr1167,882,894167,882,968

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)
nssv168920970.0181186404
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