A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993190



Internal ID20560230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62370901..62371700hg38UCSC Ensembl
chr11:62138373..62139172hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469444
Supporting Variants
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00676


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