A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17054933



Internal ID104459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3059235..3060428hg38UCSC Ensembl
chr12:3168401..3169594hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17054933
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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