A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523998



Internal ID15451291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23424644..23425882hg38UCSC Ensembl
Innerchr20:23405281..23406519hg19UCSC Ensembl
Innerchr20:23353281..23354519hg18UCSC Ensembl
Innerchr20:23353281..23354519hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381239
hg191239
hg181239
hg171239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699858
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523998
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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