A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527081



Internal ID15454374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83167484..83202742hg38UCSC Ensembl
Innerchr7:82796800..82832058hg19UCSC Ensembl
Innerchr7:82634736..82669994hg18UCSC Ensembl
Innerchr7:82441451..82476709hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3835259
hg1935259
hg1835259
hg1735259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703460
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527081
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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