A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963010



Internal ID18598252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14280561..14302972hg38UCSC Ensembl
Innerchr19:14391373..14413784hg19UCSC Ensembl
Innerchr19:14252373..14274784hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3822412
hg1922412
hg1822412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2134574, nssv2134571, nssv2134580, nssv2134578, nssv2134573, nssv2134576, nssv2134579, nssv2134575, nssv2134572, nssv2134577
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)nsv963010
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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