A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215317



Internal ID20782357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91569579..91843325hg38UCSC Ensembl
chr4:92490730..92764476hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38273747
hg19273747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380772
Supporting Variants
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215317
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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