A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1868843



Internal ID17779430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119991675..119997472hg38UCSC Ensembl
Innerchr10:121751187..121756984hg19UCSC Ensembl
Innerchr10:121741177..121746974hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg385798
hg195798
hg185798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948205
Supporting Variants
SamplesHGDP00665
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)nssv1868843
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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