A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211847



Internal ID20778887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28271558..28642058hg38UCSC Ensembl
chr4:28273180..28643680hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38370501
hg19370501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361432
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211847
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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