A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116422



Internal ID20683462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42704122..42707420hg38UCSC Ensembl
chr4:42706139..42709437hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383299
hg193299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116422
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02075


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