A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211764



Internal ID20778804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2320930..2325070hg38UCSC Ensembl
chr4:2322657..2326797hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg384141
hg194141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361168
Supporting Variants
Samples
Known GenesZFYVE28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211764
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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