A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965216



Internal ID18600450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140899895..140902473hg38UCSC Ensembl
Innerchr3:140618737..140621315hg19UCSC Ensembl
Innerchr3:142101427..142104005hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382579
hg192579
hg182579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2297089, nssv2297087, nssv2297088, nssv2297082, nssv2297080, nssv2297083, nssv2297081, nssv2297085, nssv2297086, nssv2297084
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)nsv965216
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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