A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969602



Internal ID18604829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42665222..42670963hg38UCSC Ensembl
Innerchr9:44342025..44347766hg19UCSC Ensembl
Innerchr9:44282021..44287762hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385742
hg195742
hg185742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2736223, nssv2736221, nssv2736228, nssv2736230, nssv2736224, nssv2736222, nssv2736225, nssv2736227, nssv2736229, nssv2736226
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)nsv969602
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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