A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994029



Internal ID20561069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82899901..82902400hg38UCSC Ensembl
chr11:82610943..82613442hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465150
Supporting Variants
Samples
Known GenesC11orf82, PRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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