A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523626



Internal ID15450919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:121098215..121123158hg38UCSC Ensembl
Innerchr7:120738269..120763212hg19UCSC Ensembl
Innerchr7:120525505..120550448hg18UCSC Ensembl
Innerchr7:120332220..120357163hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3824944
hg1924944
hg1824944
hg1724944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699424
Samples
Known GenesCPED1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523626
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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