A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2032352



Internal ID17783608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76471945..76473411hg38UCSC Ensembl
Innerchr15:76764286..76765752hg19UCSC Ensembl
Innerchr15:74551341..74552807hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg381467
hg191467
hg181467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974602
Supporting Variants
SamplesHGDP00665
Known GenesSCAPER
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)nssv2032352
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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