A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960515



Internal ID18595766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60564786..60567083hg38UCSC Ensembl
Innerchr17:58642147..58644444hg19UCSC Ensembl
Innerchr17:55996929..55999226hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382298
hg192298
hg182298
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2105196, nssv2105192, nssv2105198, nssv2105191, nssv2105193, nssv2105194, nssv2105195, nssv2105199, nssv2105197, nssv2105190
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)nsv960515
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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