A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523815



Internal ID15451108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4015141..4049244hg38UCSC Ensembl
Innerchr7:4054773..4088876hg19UCSC Ensembl
Innerchr7:4021299..4055402hg18UCSC Ensembl
Innerchr7:3828014..3862117hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3834104
hg1934104
hg1834104
hg1734104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699645
Samples
Known GenesSDK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523815
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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