A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965685



Internal ID18600915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:20490446..20493315hg38UCSC Ensembl
Innerchr6:20490677..20493546hg19UCSC Ensembl
Innerchr6:20598656..20601525hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382870
hg192870
hg182870
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2396540, nssv2396538, nssv2396533, nssv2396537, nssv2396534, nssv2396532, nssv2396531, nssv2396535, nssv2396536, nssv2396539
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesE2F3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965685
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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