A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17689444



Internal ID113110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80076564..80146128hg38UCSC Ensembl
chr12:80470344..80539908hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3869565
hg1969565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17689444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000313


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