A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524531



Internal ID15451824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101842610..102076908hg38UCSC Ensembl
Innerchr5:101178314..101412612hg19UCSC Ensembl
Innerchr5:101206213..101440511hg18UCSC Ensembl
Innerchr5:101206213..101440511hg17UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38234299
hg19234299
hg18234299
hg17234299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700481
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524531
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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