A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106827



Internal ID20673867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100395051..100395585hg38UCSC Ensembl
chr4:101316208..101316742hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387145
Supporting Variants
Samples
Known GenesEMCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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