A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995569



Internal ID20562609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95504001..95613900hg38UCSC Ensembl
chr11:95237165..95347064hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38109900
hg19109900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00082


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