A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960441



Internal ID18249006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20966695..20969465hg38UCSC Ensembl
Innerchr17:20870008..20872778hg19UCSC Ensembl
Innerchr17:20810600..20813370hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382771
hg192771
hg182771
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2084338, nssv2084343, nssv2084342, nssv2084337, nssv2084341, nssv2084340, nssv2084344, nssv2084335, nssv2084336, nssv2084339
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)nsv960441
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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