A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210919



Internal ID20777959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62458325..62479144hg38UCSC Ensembl
chr4:63324043..63344862hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3820820
hg1920820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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