A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985458



Internal ID20552498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102174423..102174939hg38UCSC Ensembl
chr11:102045154..102045670hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462652
Supporting Variants
Samples
Known GenesYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00044


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