A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817688



Internal ID21263026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23040251..23040382hg38UCSC Ensembl
chr8:22897764..22897895hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706419
Samples
Known GenesTNFRSF10B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817688
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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