A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1858938



Internal ID17878390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:83896516..83897236hg38UCSC Ensembl
Innerchr10:85656272..85656992hg19UCSC Ensembl
Innerchr10:85646252..85646972hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38721
hg19721
hg18721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948105
Supporting Variants
SamplesHGDP01307
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)nssv1858938
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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