A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967077



Internal ID18602306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:148164456..148168247hg38UCSC Ensembl
Innerchr3:147882243..147886034hg19UCSC Ensembl
Innerchr3:149364933..149368724hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg383792
hg193792
hg183792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2300509, nssv2300510, nssv2300507, nssv2300513, nssv2300515, nssv2300514, nssv2300508, nssv2300511, nssv2300506, nssv2300512
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)nsv967077
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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