A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963375



Internal ID18598616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:167065442..167066972hg38UCSC Ensembl
Innerchr3:166783230..166784760hg19UCSC Ensembl
Innerchr3:168265924..168267454hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381531
hg191531
hg181531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2304774, nssv2304771, nssv2304778, nssv2304775, nssv2304776, nssv2304779, nssv2304772, nssv2304770, nssv2304777, nssv2304773
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)nsv963375
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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