A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992589



Internal ID20559629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66799132..66807512hg38UCSC Ensembl
chr11:66566603..66574983hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg388381
hg198381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472084
Supporting Variants
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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