A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210924



Internal ID20777964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6265417..6293830hg38UCSC Ensembl
chr4:6267144..6295557hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3828414
hg1928414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372451
Supporting Variants
Samples
Known GenesWFS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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