A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045693



Internal ID98228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40202650..40213564hg38UCSC Ensembl
chr11:40224200..40235114hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3810915
hg1910915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513248
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045693
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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