A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972660



Internal ID18607876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32943510..32954073hg38UCSC Ensembl
Innerchr9:32943508..32954071hg19UCSC Ensembl
Innerchr9:32933508..32944071hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3810564
hg1910564
hg1810564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2526244, nssv2526235, nssv2526241, nssv2526243, nssv2526236, nssv2526238, nssv2526237, nssv2526242, nssv2526240, nssv2526239
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)nsv972660
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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