A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394630



Internal ID21052183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:123492582..123494822hg38UCSC Ensembl
chr4:124413737..124415977hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg382241
hg192241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394630
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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