A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993486



Internal ID20560526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67359711..67361287hg38UCSC Ensembl
chr11:67127182..67128758hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381577
hg191577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473356
Supporting Variants
Samples
Known GenesLOC100130987
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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