A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394571



Internal ID21052124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54372819..54383067hg38UCSC Ensembl
chr4:55238986..55249234hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3810249
hg1910249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394571
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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