A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967082



Internal ID18602311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161328946..161330434hg38UCSC Ensembl
Innerchr3:161046734..161048222hg19UCSC Ensembl
Innerchr3:162529428..162530916hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381489
hg191489
hg181489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2301441, nssv2301434, nssv2301436, nssv2301442, nssv2301438, nssv2301439, nssv2301435, nssv2301437, nssv2301433, nssv2301440
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)nsv967082
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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