A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2131829



Internal ID17819000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9310928..9324286hg38UCSC Ensembl
Innerchr19:9421604..9434962hg19UCSC Ensembl
Innerchr19:9282604..9295962hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813359
hg1913359
hg1813359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv961176
Supporting Variants
SamplesHGDP00927
Known GenesZNF559, ZNF559-ZNF177
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)nssv2131829
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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