A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981130



Internal ID18616329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32324893..32326484hg38UCSC Ensembl
Innerchr6:32292670..32294261hg19UCSC Ensembl
Innerchr6:32400648..32402239hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381592
hg191592
hg181592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2403450, nssv2403457, nssv2403448, nssv2403455, nssv2403452, nssv2403454, nssv2403451, nssv2403456, nssv2403453, nssv2403449
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC6orf10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981130
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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