A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684155



Internal ID107821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93803649..93808914hg38UCSC Ensembl
chr12:94197425..94202690hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg385266
hg195266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502626
Supporting Variants
Samples
Known GenesCRADD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684155
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002968


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