A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212547



Internal ID20779587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5723550..5770317hg38UCSC Ensembl
chr4:5725277..5772044hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3846768
hg1946768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359267
Supporting Variants
Samples
Known GenesEVC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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