A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685467



Internal ID109133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:130693512..130712050hg38UCSC Ensembl
chr12:131178057..131196595hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3818539
hg1918539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685467
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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