A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694639



Internal ID15084605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8606339..8639970hg38UCSC Ensembl
Innerchr4:8608066..8641696hg19UCSC Ensembl
Innerchr4:8658966..8692596hg18UCSC Ensembl
Innerchr4:8726137..8759767hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3833632
hg1933631
hg1833631
hg1733631
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521867
Supporting Variants
Samples
Known GenesCPZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694639
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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