A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684505



Internal ID108171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111654304..111658092hg38UCSC Ensembl
chr12:112092108..112095896hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg383789
hg193789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495899
Supporting Variants
Samples
Known GenesBRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684505
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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