A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966994



Internal ID18602223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17874136..17879900hg38UCSC Ensembl
Innerchr3:17915628..17921392hg19UCSC Ensembl
Innerchr3:17890632..17896396hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385765
hg195765
hg185765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2275951, nssv2275954, nssv2275946, nssv2275947, nssv2275948, nssv2275952, nssv2275953, nssv2275949, nssv2275955, nssv2275950
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)nsv966994
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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