A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361432



Internal ID21018985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28271558..28642058hg38UCSC Ensembl
chr4:28273180..28643680hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38370501
hg19370501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361432
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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