A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992590



Internal ID20559630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66826971..66832335hg38UCSC Ensembl
chr11:66594442..66599806hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385365
hg195365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470636
Supporting Variants
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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