A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695713



Internal ID15085679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8609449..8618737hg38UCSC Ensembl
Innerchr4:8611176..8620464hg19UCSC Ensembl
Innerchr4:8662076..8671364hg18UCSC Ensembl
Innerchr4:8729247..8738535hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg389289
hg199289
hg189289
hg179289
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518282
Supporting Variants
Samples
Known GenesCPZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695713
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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