A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965686



Internal ID18600916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:23852447..23856866hg38UCSC Ensembl
Innerchr6:23852675..23857094hg19UCSC Ensembl
Innerchr6:23960654..23965073hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg384420
hg194420
hg184420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2705250, nssv2396631, nssv2705244, nssv2705241, nssv2396634, nssv2396629, nssv2396636, nssv2705249, nssv2705242, nssv2705248, nssv2396635, nssv2396633, nssv2705246, nssv2705243, nssv2396628, nssv2705245, nssv2396632, nssv2396637, nssv2705247, nssv2396630
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965686
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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