A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995425



Internal ID20562465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9590304..9602275hg38UCSC Ensembl
chr11:9611851..9623822hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811972
hg1911972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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