A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697237



Internal ID15433889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:158220308..158228036hg38UCSC Ensembl
Innerchr5:157647316..157655044hg19UCSC Ensembl
Innerchr5:157579894..157587622hg18UCSC Ensembl
Innerchr5:157579894..157587622hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg387729
hg197729
hg187729
hg177729
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520127
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697237
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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