A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1860029



Internal ID17779036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84555724..84570473hg38UCSC Ensembl
Innerchr10:86315480..86330229hg19UCSC Ensembl
Innerchr10:86305460..86320209hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3814750
hg1914750
hg1814750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948108
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)nssv1860029
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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