A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700824



Internal ID15090790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:147085516..147186485hg38UCSC Ensembl
Innerchr5:146465079..146566048hg19UCSC Ensembl
Innerchr5:146445272..146546241hg18UCSC Ensembl
Innerchr5:146445272..146546241hg17UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38100970
hg19100970
hg18100970
hg17100970
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519847
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700824
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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