A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696418



Internal ID15433070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:171875550..171962723hg38UCSC Ensembl
Innerchr3:171593340..171680513hg19UCSC Ensembl
Innerchr3:173076034..173163207hg18UCSC Ensembl
Innerchr3:173076042..173163215hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3887174
hg1987174
hg1887174
hg1787174
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518951
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696418
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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