A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945853



Internal ID18592703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28095147..28096377hg38UCSC Ensembl
Innerchr1:28421658..28422888hg19UCSC Ensembl
Innerchr1:28294245..28295475hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381231
hg191231
hg181231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1757759, nssv1757761, nssv1757758, nssv1757765, nssv1757760, nssv1757764, nssv1757766, nssv1757757, nssv1757762, nssv1757763
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)nsv945853
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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