A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965683



Internal ID18600913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19142767..19145583hg38UCSC Ensembl
Innerchr6:19142998..19145814hg19UCSC Ensembl
Innerchr6:19250977..19253793hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382817
hg192817
hg182817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2395814, nssv2395815, nssv2395811, nssv2395809, nssv2395810, nssv2395817, nssv2395816, nssv2395818, nssv2395813, nssv2395812
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)nsv965683
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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