A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518461



Internal ID15445754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21104379..21108059hg38UCSC Ensembl
Innerchr7:21143998..21147678hg19UCSC Ensembl
Innerchr7:21110523..21114203hg18UCSC Ensembl
Innerchr7:20917238..20920918hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383681
hg193681
hg183681
hg173681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695898
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518461
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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