A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050414



Internal ID101498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117307372..117309942hg38UCSC Ensembl
chr11:117178088..117180658hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382571
hg192571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499739
Supporting Variants
Samples
Known GenesBACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050414
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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