A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688759



Internal ID112425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67231518..67231610hg38UCSC Ensembl
chr12:67625298..67625390hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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