A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2014968



Internal ID17864020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28664471..28667892hg38UCSC Ensembl
Innerchr15:28909617..28913038hg19UCSC Ensembl
Innerchr15:26708658..26712079hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg383422
hg193422
hg183422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv977683
Supporting Variants
SamplesHGDP01284
Known GenesHERC2P9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2014968
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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