A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523515



Internal ID15450808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45685097..45696087hg38UCSC Ensembl
Innerchr7:45724696..45735686hg19UCSC Ensembl
Innerchr7:45691221..45702211hg18UCSC Ensembl
Innerchr7:45497936..45508926hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3810991
hg1910991
hg1810991
hg1710991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699288
Samples
Known GenesADCY1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523515
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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