A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989497



Internal ID20556537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21998950..22101335hg38UCSC Ensembl
chr11:22020496..22122881hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38102386
hg19102386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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