A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2033785



Internal ID17863914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79556484..79560451hg38UCSC Ensembl
Innerchr15:79848826..79852793hg19UCSC Ensembl
Innerchr15:77635881..77639848hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383968
hg193968
hg183968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976955
Supporting Variants
SamplesHGDP01284
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)nssv2033785
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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