A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699004



Internal ID15435656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:157960148..157967798hg38UCSC Ensembl
Innerchr5:157387156..157394806hg19UCSC Ensembl
Innerchr5:157319734..157327384hg18UCSC Ensembl
Innerchr5:157319734..157327384hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg387651
hg197651
hg187651
hg177651
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523270
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699004
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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