A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981096



Internal ID18616295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:336244..347399hg38UCSC Ensembl
Innerchr6:336244..347399hg19UCSC Ensembl
Innerchr6:281244..292399hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3811156
hg1911156
hg1811156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2391770, nssv2391773, nssv2391774, nssv2391771, nssv2391777, nssv2391779, nssv2391775, nssv2391776, nssv2391778, nssv2391772
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDUSP22
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981096
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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