A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969403



Internal ID18604630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55938995..55941378hg38UCSC Ensembl
Innerchr6:55803793..55806176hg19UCSC Ensembl
Innerchr6:55911752..55914135hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg382384
hg192384
hg182384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2410467, nssv2410463, nssv2410462, nssv2410460, nssv2410466, nssv2410468, nssv2410464, nssv2410459, nssv2410465, nssv2410461
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)nsv969403
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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