A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2029793



Internal ID17832501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67985095..67986648hg38UCSC Ensembl
Innerchr15:68277433..68278986hg19UCSC Ensembl
Innerchr15:66064487..66066040hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381554
hg191554
hg181554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976945
Supporting Variants
SamplesHGDP00998
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)nssv2029793
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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