A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993222



Internal ID20560262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62668393..62668676hg38UCSC Ensembl
chr11:62435865..62436148hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464545
Supporting Variants
Samples
Known GenesC11orf48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993222
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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