A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213534



Internal ID20780574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3582302..3709179hg38UCSC Ensembl
chr4:3584029..3710906hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38126878
hg19126878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364236
Supporting Variants
Samples
Known GenesLINC00955, LOC100133461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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