A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690109



Internal ID113775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96640564..96674564hg38UCSC Ensembl
chr12:97034342..97068342hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3834001
hg1934001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690109
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000313


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