A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972703



Internal ID18607919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40362627..40468937hg38UCSC Ensembl
Innerchr9:42507645..42613955hg19UCSC Ensembl
Innerchr9:42497641..42604076hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38106311
hg19106311
hg18106436
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2536310, nssv2536314, nssv2536313, nssv2536315, nssv2536308, nssv2536309, nssv2536307, nssv2536312, nssv2536311, nssv2536306
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972703
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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