A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962331



Internal ID18597575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:47011077..47064378hg38UCSC Ensembl
Innerchr17:45088443..45141744hg19UCSC Ensembl
Innerchr17:42443442..42496743hg18UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3853302
hg1953302
hg1853302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2099311, nssv2099307, nssv2099309, nssv2099314, nssv2099308, nssv2099315, nssv2099312, nssv2099313, nssv2099316, nssv2099310
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)nsv962331
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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