A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686775



Internal ID110441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33689523..33689600hg38UCSC Ensembl
chr13:34263660..34263737hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497889
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686775
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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