A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121797



Internal ID20688837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87846280..87846995hg38UCSC Ensembl
chr4:88767432..88768147hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38716
hg19716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393987
Supporting Variants
Samples
Known GenesMEPE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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