A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960830



Internal ID18596077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35957040..35960305hg38UCSC Ensembl
Innerchr19:36447942..36451207hg19UCSC Ensembl
Innerchr19:41139782..41143047hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383266
hg193266
hg183266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2146282, nssv2146283, nssv2146281, nssv2146279, nssv2146286, nssv2146285, nssv2146284, nssv2146280, nssv2146277, nssv2146278
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)nsv960830
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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