A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524661



Internal ID15451954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16759952..16767921hg38UCSC Ensembl
Innerchr20:16740597..16748566hg19UCSC Ensembl
Innerchr20:16688597..16696566hg18UCSC Ensembl
Innerchr20:16688597..16696566hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg387970
hg197970
hg187970
hg177970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700630
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524661
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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