A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995019



Internal ID20562059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88110435..88112644hg38UCSC Ensembl
chr11:87843603..87845812hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382210
hg192210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465928
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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