A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213879



Internal ID20780919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170158301..170170300hg38UCSC Ensembl
chr4:171079452..171091451hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3812000
hg1912000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213879
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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