A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979812



Internal ID18615013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27213309..27214872hg38UCSC Ensembl
Innerchr3:27254800..27256363hg19UCSC Ensembl
Innerchr3:27229804..27231367hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381564
hg191564
hg181564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2275356, nssv2275360, nssv2275355, nssv2275354, nssv2275358, nssv2275353, nssv2275357, nssv2275359, nssv2275351, nssv2275352
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)nsv979812
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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