A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057236



Internal ID106005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32133435..32142314hg38UCSC Ensembl
chr12:32286369..32295248hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg388880
hg198880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501075
Supporting Variants
Samples
Known GenesBICD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057236
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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