A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990804



Internal ID20557844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33713804..33714309hg38UCSC Ensembl
chr11:33735350..33735855hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467096
Supporting Variants
Samples
Known GenesCD59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00091


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