A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688792



Internal ID112458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67722853..67722918hg38UCSC Ensembl
chr12:68116633..68116698hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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