A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695566



Internal ID119232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109798280..109798462hg38UCSC Ensembl
chr13:110450627..110450809hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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