A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986999



Internal ID20554039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115388630..115407662hg38UCSC Ensembl
chr11:115259348..115278380hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3819033
hg1919033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458539
Supporting Variants
Samples
Known GenesCADM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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