A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2012955



Internal ID17734928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25946718..25954534hg38UCSC Ensembl
Innerchr15:26191865..26199681hg19UCSC Ensembl
Innerchr15:23742958..23750774hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg387817
hg197817
hg187817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974535
Supporting Variants
SamplesHGDP00456
Known GenesLOC100128714
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)nssv2012955
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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