A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989331



Internal ID20556371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21688468..21695397hg38UCSC Ensembl
chr11:21710014..21716943hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg386930
hg196930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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