A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992958



Internal ID20559998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80292980..80293588hg38UCSC Ensembl
chr11:80004024..80004632hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00035


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