A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1859687



Internal ID17812104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80212303..80235396hg38UCSC Ensembl
Innerchr10:81972059..81995152hg19UCSC Ensembl
Innerchr10:81962039..81985132hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3823094
hg1923094
hg1823094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948100
Supporting Variants
SamplesHGDP00927
Known GenesLINC00857
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)nssv1859687
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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