A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107779



Internal ID20674819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109876751..109882780hg38UCSC Ensembl
chr4:110797907..110803936hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg386030
hg196030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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