A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2033233



Internal ID17384754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79742169..79744968hg38UCSC Ensembl
Innerchr15:80034511..80037310hg19UCSC Ensembl
Innerchr15:77821566..77824365hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382800
hg192800
hg182800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974608
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)nssv2033233
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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