A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712811



Internal ID136477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35482907..35501429hg38UCSC Ensembl
chr17:33809926..33828448hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3818523
hg1918523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522806
Supporting Variants
Samples
Known GenesSLFN12L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712811
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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