A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969583



Internal ID18604810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61172321..61175835hg38UCSC Ensembl
Innerchr9:43644940..43648119hg19UCSC Ensembl
Innerchr9:43584936..43588115hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383515
hg193180
hg183180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2735247, nssv2735246, nssv2735239, nssv2735238, nssv2735245, nssv2735242, nssv2735241, nssv2735240, nssv2735244, nssv2735243
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969583
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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