A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688314



Internal ID111980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61203036..61203231hg38UCSC Ensembl
chr13:61777170..61777365hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688314
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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