A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525482



Internal ID15106089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129250971..129405350hg38UCSC Ensembl
Innerchr7:128890812..129045191hg19UCSC Ensembl
Innerchr7:128678048..128832427hg18UCSC Ensembl
Innerchr7:128484763..128639142hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38154380
hg19154380
hg18154380
hg17154380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701610
Samples
Known GenesAHCYL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525482
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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