A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965935



Internal ID18601165
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764583, nssv2761621
SamplesHGDP00456, HGDP00927
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965935
Frequency
Sample Size10
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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