A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211152



Internal ID20778192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:162159101..162249900hg38UCSC Ensembl
chr4:163080253..163171052hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3890800
hg1990800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388614
Supporting Variants
Samples
Known GenesFSTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211152
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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