A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973297



Internal ID18608512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62519679..62566414hg38UCSC Ensembl
Innerchr9:46830980..46877715hg19UCSC Ensembl
Innerchr9:46670976..46717711hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg3846736
hg1946736
hg1846736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2737670, nssv2737677, nssv2737678, nssv2737675, nssv2737672, nssv2737671, nssv2737676, nssv2737673, nssv2737669, nssv2737674
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC643648
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973297
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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