A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969604



Internal ID18604831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42670963..42675671hg38UCSC Ensembl
Innerchr9:44347766..44352469hg19UCSC Ensembl
Innerchr9:44287762..44292465hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384709
hg194704
hg184704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2736239, nssv2736234, nssv2736233, nssv2736242, nssv2736236, nssv2736240, nssv2736235, nssv2736238, nssv2736237, nssv2736241
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)nsv969604
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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