A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112408



Internal ID20679448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174011937..174012577hg38UCSC Ensembl
chr4:174933088..174933728hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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