A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2014897



Internal ID17785794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28624719..28659180hg38UCSC Ensembl
Innerchr15:28869865..28904326hg19UCSC Ensembl
Innerchr15:26668906..26703367hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3834462
hg1934462
hg1834462
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976908
Supporting Variants
SamplesHGDP00665
Known GenesHERC2P9
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)nssv2014897
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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