A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960825



Internal ID18596072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33359305..33363812hg38UCSC Ensembl
Innerchr19:33850211..33854718hg19UCSC Ensembl
Innerchr19:38542051..38546558hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384508
hg194508
hg184508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2144806, nssv2144811, nssv2144810, nssv2144808, nssv2144809, nssv2144805, nssv2144813, nssv2144814, nssv2144812, nssv2144807
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)nsv960825
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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