A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522909



Internal ID15450202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4285098..4444226hg38UCSC Ensembl
Innerchr7:4324730..4483857hg19UCSC Ensembl
Innerchr7:4291256..4450383hg18UCSC Ensembl
Innerchr7:4097971..4257098hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38159129
hg19159128
hg18159128
hg17159128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698568
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522909
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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