A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1865516



Internal ID17762853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93206658..93212080hg38UCSC Ensembl
Innerchr10:94966415..94971837hg19UCSC Ensembl
Innerchr10:94956405..94961827hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385423
hg195423
hg185423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948141
Supporting Variants
SamplesHGDP00542
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)nssv1865516
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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