A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526616



Internal ID15107223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:81513586..82297077hg38UCSC Ensembl
Innerchr4:82434740..83218230hg19UCSC Ensembl
Innerchr4:82653764..83437254hg18UCSC Ensembl
Innerchr4:82791919..83575409hg17UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38783492
hg19783491
hg18783491
hg17783491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702936
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526616
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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