A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209451



Internal ID20776491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103096823..103120143hg38UCSC Ensembl
chr4:104017980..104041300hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3823321
hg1923321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390567
Supporting Variants
Samples
Known GenesBDH2, CENPE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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