A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963037



Internal ID18598279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33336509..33344158hg38UCSC Ensembl
Innerchr19:33827415..33835064hg19UCSC Ensembl
Innerchr19:38519255..38526904hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg387650
hg197650
hg187650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2143525, nssv2143522, nssv2143520, nssv2143521, nssv2143518, nssv2143519, nssv2143516, nssv2143523, nssv2143517, nssv2143524
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)nsv963037
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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