A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987234



Internal ID20554276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119609742..119610395hg38UCSC Ensembl
chr11:119480454..119481107hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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