A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968712



Internal ID18603940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82052879..82067334hg38UCSC Ensembl
Innerchr9:84667794..84682249hg19UCSC Ensembl
Innerchr9:83857614..83872069hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3814456
hg1914456
hg1814456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2554324, nssv2554315, nssv2554316, nssv2554320, nssv2554317, nssv2554323, nssv2554318, nssv2554322, nssv2554321, nssv2554319
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)nsv968712
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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