A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392692



Internal ID21050245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109234672..109474012hg38UCSC Ensembl
chr4:110155828..110395168hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38239341
hg19239341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209516
Samples
Known GenesCOL25A1, SEC24B, SEC24B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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