A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045729



Internal ID98253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40771827..40835186hg38UCSC Ensembl
chr11:40793377..40856736hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3863360
hg1963360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502122
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045729
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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