A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2764583



Internal ID17823336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23187502..23194767hg38UCSC Ensembl
Innerchr20:23168139..23175404hg19UCSC Ensembl
Innerchr20:23116139..23123404hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg387266
hg197266
hg187266
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv965935
Supporting Variants
SamplesHGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2764583
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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