A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521129



Internal ID15448422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10497229..10606265hg38UCSC Ensembl
Innerchr7:10536856..10645892hg19UCSC Ensembl
Innerchr7:10503381..10612417hg18UCSC Ensembl
Innerchr7:10310096..10419132hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38109037
hg19109037
hg18109037
hg17109037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694418
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521129
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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