A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966999



Internal ID18602228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31452912..31455720hg38UCSC Ensembl
Innerchr3:31494404..31497212hg19UCSC Ensembl
Innerchr3:31469408..31472216hg18UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg382809
hg192809
hg182809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2276369, nssv2276370, nssv2276365, nssv2276371, nssv2276368, nssv2276366, nssv2276367, nssv2276362, nssv2276363, nssv2276364
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)nsv966999
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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