A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965235



Internal ID18600469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178492786..178494000hg38UCSC Ensembl
Innerchr3:178210574..178211788hg19UCSC Ensembl
Innerchr3:179693268..179694482hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg381215
hg191215
hg181215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2298690, nssv2298691, nssv2298694, nssv2298685, nssv2298686, nssv2298687, nssv2298693, nssv2298688, nssv2298689, nssv2298692
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)nsv965235
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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