A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1863508



Internal ID17482201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96914584..96917068hg38UCSC Ensembl
Innerchr10:98674341..98676825hg19UCSC Ensembl
Innerchr10:98664331..98666815hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382485
hg192485
hg182485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948154
Supporting Variants
SamplesHGDP00998
Known GenesLCOR
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)nssv1863508
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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