A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526637



Internal ID15453930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9951307..9957921hg38UCSC Ensembl
Innerchr18:9951304..9957918hg19UCSC Ensembl
Innerchr18:9941304..9947918hg18UCSC Ensembl
Innerchr18:9941304..9947918hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg386615
hg196615
hg186615
hg176615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702959
Samples
Known GenesVAPA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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