A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210304



Internal ID20777344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128528345..128709802hg38UCSC Ensembl
chr4:129449500..129630957hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38181458
hg19181458
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210304
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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