A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963393



Internal ID18598634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194562223..194563900hg38UCSC Ensembl
Innerchr3:194282952..194284629hg19UCSC Ensembl
Innerchr3:195764241..195765918hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381678
hg191678
hg181678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2307216, nssv2307217, nssv2307210, nssv2307215, nssv2307209, nssv2307218, nssv2307212, nssv2307211, nssv2307214, nssv2307213
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)nsv963393
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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