A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520737



Internal ID15101344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2951975..2967728hg38UCSC Ensembl
Innerchr8:2809497..2825250hg19UCSC Ensembl
Innerchr8:2796904..2812657hg18UCSC Ensembl
Innerchr8:2796904..2812657hg17UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg3815754
hg1915754
hg1815754
hg1715754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674863, nssv692906
Samples
Known GenesCSMD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520737
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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