A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965231



Internal ID18600465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:167693057..167694547hg38UCSC Ensembl
Innerchr3:167410845..167412335hg19UCSC Ensembl
Innerchr3:168893539..168895029hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381491
hg191491
hg181491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2303565, nssv2302764, nssv2303564, nssv2303561, nssv2303562, nssv2303560, nssv2303563, nssv2302765, nssv2302766, nssv2303559
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPDCD10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965231
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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