A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981109



Internal ID18616308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:20041912..20044030hg38UCSC Ensembl
Innerchr6:20042143..20044261hg19UCSC Ensembl
Innerchr6:20150122..20152240hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382119
hg192119
hg182119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2396097, nssv2396095, nssv2396093, nssv2396099, nssv2396101, nssv2396100, nssv2396094, nssv2396096, nssv2396092, nssv2396098
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)nsv981109
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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