A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2038574



Internal ID17734310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99551254..99552068hg38UCSC Ensembl
Innerchr15:100091459..100092273hg19UCSC Ensembl
Innerchr15:97908982..97909796hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38815
hg19815
hg18815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976969
Supporting Variants
SamplesHGDP00456
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)nssv2038574
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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