A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379636



Internal ID21037189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125809348..125812328hg38UCSC Ensembl
chr4:126730503..126733483hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg382981
hg192981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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