A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979841



Internal ID18268356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72885057..72886057hg38UCSC Ensembl
Innerchr3:72934208..72935208hg19UCSC Ensembl
Innerchr3:73016898..73017898hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2282416, nssv2282413, nssv2282421, nssv2282417, nssv2282414, nssv2282412, nssv2282415, nssv2282420, nssv2282419, nssv2282418
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)nsv979841
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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