A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992938



Internal ID20559978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80166260..80166732hg38UCSC Ensembl
chr11:79877304..79877776hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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