A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995533



Internal ID20562573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94884813..94885880hg38UCSC Ensembl
chr11:94617978..94619045hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464183
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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