A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211607



Internal ID20778647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:659530..680018hg38UCSC Ensembl
chr4:653319..673807hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3820489
hg1920489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366925
Supporting Variants
Samples
Known GenesATP5I, MYL5, PDE6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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