A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2025272



Internal ID17784424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59045777..59051886hg38UCSC Ensembl
Innerchr15:59337976..59344085hg19UCSC Ensembl
Innerchr15:57125268..57131377hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg386110
hg196110
hg186110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984077
Supporting Variants
SamplesHGDP00665
Known GenesRNF111
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)nssv2025272
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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