A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989846



Internal ID20556886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27987159..27987513hg38UCSC Ensembl
chr11:28008706..28009060hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00125


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