A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963017



Internal ID18598259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18031679..18032179hg38UCSC Ensembl
Innerchr19:18142489..18142989hg19UCSC Ensembl
Innerchr19:18003489..18003989hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2137924, nssv2137922, nssv2137917, nssv2137920, nssv2137919, nssv2137918, nssv2137923, nssv2137921, nssv2137925, nssv2137916
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)nsv963017
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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