A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2020809



Internal ID17749634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43115707..43118617hg38UCSC Ensembl
Innerchr15:43407905..43410815hg19UCSC Ensembl
Innerchr15:41195197..41198107hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg382911
hg192911
hg182911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984061
Supporting Variants
SamplesHGDP00521
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)nssv2020809
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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