A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993017



Internal ID20560057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80935601..80936500hg38UCSC Ensembl
chr11:80646644..80647543hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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