A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418657



Internal ID22476527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18119248..18125802hg38UCSC Ensembl
chr4:18120871..18127425hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386555
hg196555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418657
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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