A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969454



Internal ID18604681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148566783..148567648hg38UCSC Ensembl
Innerchr6:148887919..148888784hg19UCSC Ensembl
Innerchr6:148929612..148930477hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38866
hg19866
hg18866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2426389, nssv2425688, nssv2426388, nssv2426387, nssv2426384, nssv2426386, nssv2425689, nssv2425690, nssv2425691, nssv2426385
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)nsv969454
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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