A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392426



Internal ID21049979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62446990..62522478hg38UCSC Ensembl
chr4:63312708..63388196hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3875489
hg1975489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210918
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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