A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995580



Internal ID20562620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95588556..95589030hg38UCSC Ensembl
chr11:95321720..95322194hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00099


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