A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996309



Internal ID20563350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89113884..89114322hg38UCSC Ensembl
chr11:88847052..88847490hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473750
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996309
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00027


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