A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981159



Internal ID18616358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:79353238..79354803hg38UCSC Ensembl
Innerchr6:80062955..80064520hg19UCSC Ensembl
Innerchr6:80119674..80121239hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381566
hg191566
hg181566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2416306, nssv2416313, nssv2416312, nssv2416314, nssv2416309, nssv2416307, nssv2416305, nssv2416311, nssv2416308, nssv2416310
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)nsv981159
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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