A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963338



Internal ID18598579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80441368..80442767hg38UCSC Ensembl
Innerchr3:80490518..80491917hg19UCSC Ensembl
Innerchr3:80573208..80574607hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381400
hg191400
hg181400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2286317, nssv2286313, nssv2286318, nssv2286312, nssv2286315, nssv2286316, nssv2286311, nssv2286320, nssv2286314, nssv2286319
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)nsv963338
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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