A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684534



Internal ID108200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112068993..112071892hg38UCSC Ensembl
chr12:112506797..112509696hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503444
Supporting Variants
Samples
Known GenesNAA25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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