A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979808



Internal ID18615009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18905298..18910787hg38UCSC Ensembl
Innerchr3:18946790..18952279hg19UCSC Ensembl
Innerchr3:18921794..18927283hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385490
hg195490
hg185490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2272288, nssv2272294, nssv2272291, nssv2272289, nssv2272287, nssv2272285, nssv2272290, nssv2272286, nssv2272293, nssv2272292
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)nsv979808
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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