A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961190



Internal ID18596436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14941526..14942220hg38UCSC Ensembl
Innerchr19:15052338..15053032hg19UCSC Ensembl
Innerchr19:14913338..14914032hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38695
hg19695
hg18695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2134889, nssv2134887, nssv2134883, nssv2134885, nssv2134892, nssv2134888, nssv2134891, nssv2134884, nssv2134886, nssv2134890
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR7C2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961190
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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