A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2015041



Internal ID17835861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28673820..28729293hg38UCSC Ensembl
Innerchr15:28918966..28974439hg19UCSC Ensembl
Innerchr15:26718007..26773480hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3855474
hg1955474
hg1855474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977684
Supporting Variants
SamplesHGDP00998
Known GenesGOLGA8M, HERC2P9
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)nssv2015041
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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