A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965194



Internal ID18600428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106898352..106898958hg38UCSC Ensembl
Innerchr3:106617199..106617805hg19UCSC Ensembl
Innerchr3:108099889..108100495hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38607
hg19607
hg18607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2292932, nssv2292928, nssv2292929, nssv2292933, nssv2292935, nssv2292936, nssv2292937, nssv2292934, nssv2292930, nssv2292931
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)nsv965194
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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