A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112524



Internal ID20679564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167393702..167394505hg38UCSC Ensembl
chr4:168314853..168315656hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112524
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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