A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521603



Internal ID15448896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:27719865..27729450hg38UCSC Ensembl
Innerchr18:25299829..25309414hg19UCSC Ensembl
Innerchr18:23553827..23563412hg18UCSC Ensembl
Innerchr18:23553827..23563412hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg389586
hg199586
hg189586
hg179586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698219
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521603
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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