A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965182



Internal ID18600416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82318687..82326614hg38UCSC Ensembl
Innerchr3:82367838..82375765hg19UCSC Ensembl
Innerchr3:82450528..82458455hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg387928
hg197928
hg187928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2287001, nssv2286996, nssv2287002, nssv2286998, nssv2286994, nssv2286997, nssv2286993, nssv2286999, nssv2286995, nssv2287000
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)nsv965182
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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