A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972641



Internal ID18261171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4711171..4713505hg38UCSC Ensembl
Innerchr9:4711171..4713505hg19UCSC Ensembl
Innerchr9:4701171..4703505hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382335
hg192335
hg182335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2520136, nssv2520127, nssv2520135, nssv2520131, nssv2520134, nssv2520129, nssv2520130, nssv2520128, nssv2520132, nssv2520133
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAK3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972641
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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