A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664527



Internal ID15401179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45726581..45749938hg38UCSC Ensembl
Innerchr20:44355220..44378577hg19UCSC Ensembl
Innerchr20:43788634..43811984hg18UCSC Ensembl
Innerchr20:43788634..43811984hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3823358
hg1923358
hg1823351
hg1723351
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517420
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664527
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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