A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989360



Internal ID20556400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14998301..15001200hg38UCSC Ensembl
chr11:15019847..15022746hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00134


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