A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057829



Internal ID106408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57353111..57355195hg38UCSC Ensembl
chr12:57746894..57748978hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg382085
hg192085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057829
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003592


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