A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2029372



Internal ID17884906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68253596..68257359hg38UCSC Ensembl
Innerchr15:68545934..68549697hg19UCSC Ensembl
Innerchr15:66332988..66336751hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383764
hg193764
hg183764
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984087
Supporting Variants
SamplesHGDP01307
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)nssv2029372
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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