A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690065



Internal ID113731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95794872..95797566hg38UCSC Ensembl
chr12:96188650..96191344hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382695
hg192695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690065
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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