A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391952



Internal ID21049505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105554484..105666351hg38UCSC Ensembl
chr4:106475641..106587508hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38111868
hg19111868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209477
Samples
Known GenesARHGEF38, ARHGEF38-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391952
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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