A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17058696



Internal ID106994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53634963..53637124hg38UCSC Ensembl
chr12:54028747..54030908hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg382162
hg192162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17058696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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