A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108874



Internal ID20675914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145353201..145367700hg38UCSC Ensembl
chr4:146274353..146288852hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3814500
hg1914500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00247


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