A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690706



Internal ID114372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113057435..113057848hg38UCSC Ensembl
chr12:113495240..113495653hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690706
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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