A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111585



Internal ID20678625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155289421..155289809hg38UCSC Ensembl
chr4:156210573..156210961hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392010
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00096


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