A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687359



Internal ID111025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44704630..44710507hg38UCSC Ensembl
chr13:45278766..45284643hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg385878
hg195878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500056
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687359
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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