A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528667



Internal ID15455960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7531947..7545820hg38UCSC Ensembl
Innerchr4:7533674..7547547hg19UCSC Ensembl
Innerchr4:7584574..7598447hg18UCSC Ensembl
Innerchr4:7651745..7665618hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3813874
hg1913874
hg1813874
hg1713874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705305
Samples
Known GenesSORCS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528667
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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