A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517812



Internal ID15445105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140309532..140310308hg38UCSC Ensembl
Innerchr7:140009332..140010108hg19UCSC Ensembl
Innerchr7:139655801..139656577hg18UCSC Ensembl
Innerchr7:139462516..139463292hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38777
hg19777
hg18777
hg17777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695217
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517812
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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