A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989799



Internal ID20556839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27232400..27233449hg38UCSC Ensembl
chr11:27253947..27254996hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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