A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962336



Internal ID18250894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:48070238..48072353hg38UCSC Ensembl
Innerchr17:46147600..46149715hg19UCSC Ensembl
Innerchr17:43502599..43504714hg18UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg382116
hg192116
hg182116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2100783, nssv2100786, nssv2100781, nssv2100787, nssv2100788, nssv2100785, nssv2100782, nssv2100780, nssv2100779, nssv2100784
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBX1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962336
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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