A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1859924



Internal ID17878452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84387445..84392170hg38UCSC Ensembl
Innerchr10:86147201..86151926hg19UCSC Ensembl
Innerchr10:86137181..86141906hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384726
hg194726
hg184726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948107
Supporting Variants
SamplesHGDP01307
Known GenesCCSER2
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)nssv1859924
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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