A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707546



Internal ID21229341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58165895..58166230hg38UCSC Ensembl
chr8:59078454..59078789hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818940
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707546
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.859375


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