A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692249



Internal ID115915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102946671..102951191hg38UCSC Ensembl
chr13:103599021..103603541hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg384521
hg194521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512713
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692249
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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