A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2128276



Internal ID17732832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:168900..190564hg38UCSC Ensembl
Innerchr19:168900..190564hg19UCSC Ensembl
Innerchr19:119900..141564hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3821665
hg1921665
hg1821665
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv962990
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2128276
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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