A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2137202



Internal ID17788204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15903160..15911343hg38UCSC Ensembl
Innerchr19:16013970..16022153hg19UCSC Ensembl
Innerchr19:15874970..15883153hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg388184
hg198184
hg188184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv963015
Supporting Variants
SamplesHGDP00665
Known Genes
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)nssv2137202
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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