A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110836



Internal ID20677876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14415726..14431828hg38UCSC Ensembl
chr4:14417350..14433452hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3816103
hg1916103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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