A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985109



Internal ID20552149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100813782..100828836hg38UCSC Ensembl
chr11:100684513..100699567hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3815055
hg1915055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467234
Supporting Variants
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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