A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2034841



Internal ID17788704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83195045..83195665hg38UCSC Ensembl
Innerchr15:83863797..83864417hg19UCSC Ensembl
Innerchr15:81654801..81655421hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38621
hg19621
hg18621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984103
Supporting Variants
SamplesHGDP00665
Known GenesHDGFRP3
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)nssv2034841
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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