A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991792



Internal ID20558832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4683958..4688381hg38UCSC Ensembl
chr11:4705188..4709611hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384424
hg194424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447188
Supporting Variants
Samples
Known GenesOR51E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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