A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965741



Internal ID18600971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:79952801..79953987hg38UCSC Ensembl
Innerchr6:80662518..80663704hg19UCSC Ensembl
Innerchr6:80719237..80720423hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381187
hg191187
hg181187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2416408, nssv2416403, nssv2416405, nssv2416402, nssv2416410, nssv2416404, nssv2416407, nssv2416409, nssv2416406, nssv2416411
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)nsv965741
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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