A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967000



Internal ID18602229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31986079..31996187hg38UCSC Ensembl
Innerchr3:32027571..32037679hg19UCSC Ensembl
Innerchr3:32002575..32012683hg18UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3810109
hg1910109
hg1810109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2276462, nssv2276467, nssv2276461, nssv2276460, nssv2276466, nssv2276463, nssv2276465, nssv2276468, nssv2276464, nssv2276459
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF860
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967000
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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