A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967034



Internal ID18602263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87319851..87324402hg38UCSC Ensembl
Innerchr3:87369001..87373552hg19UCSC Ensembl
Innerchr3:87451691..87456242hg18UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg384552
hg194552
hg184552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2287580, nssv2287577, nssv2287574, nssv2287573, nssv2287578, nssv2287575, nssv2287571, nssv2287576, nssv2287572, nssv2287579
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)nsv967034
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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