A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965193



Internal ID18253741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:101576002..101578566hg38UCSC Ensembl
Innerchr3:101294846..101297410hg19UCSC Ensembl
Innerchr3:102777536..102780100hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg382565
hg192565
hg182565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2290588, nssv2290592, nssv2290589, nssv2290594, nssv2290586, nssv2290587, nssv2290595, nssv2290591, nssv2290590, nssv2290593
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPCNP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965193
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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