A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211061



Internal ID20778101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133977980..133996715hg38UCSC Ensembl
chr4:134899135..134917870hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3818736
hg1918736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211061
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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