A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965189



Internal ID18600423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96616552..96618438hg38UCSC Ensembl
Innerchr3:96335396..96337282hg19UCSC Ensembl
Innerchr3:97818086..97819972hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381887
hg191887
hg181887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2291658, nssv2291662, nssv2291663, nssv2291657, nssv2291659, nssv2291665, nssv2291660, nssv2291661, nssv2291664, nssv2291656
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)nsv965189
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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