A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2138219



Internal ID17381560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15949029..15949639hg38UCSC Ensembl
Innerchr19:16059839..16060449hg19UCSC Ensembl
Innerchr19:15920839..15921449hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38611
hg19611
hg18611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv960803
Supporting Variants
SamplesHGDP00456
Known GenesOR10H4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2138219
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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