A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986760



Internal ID20553800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111473251..111473970hg38UCSC Ensembl
chr11:111343976..111344695hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468566
Supporting Variants
Samples
Known GenesBTG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986760
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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