A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210916



Internal ID20777956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6238107..6302670hg38UCSC Ensembl
chr4:6239834..6304397hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3864564
hg1964564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357193
Supporting Variants
Samples
Known GenesWFS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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