A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967020



Internal ID18602249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:70751253..70753098hg38UCSC Ensembl
Innerchr3:70800404..70802249hg19UCSC Ensembl
Innerchr3:70883094..70884939hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381846
hg191846
hg181846
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2285160, nssv2285164, nssv2285162, nssv2285163, nssv2285165, nssv2285159, nssv2285167, nssv2285161, nssv2285166, nssv2285168
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)nsv967020
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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