A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755584



Internal ID20531444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38627496..38627496hg38UCSC Ensembl
chr20:37256139..37256139hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293155
Samples
Known GenesARHGAP40
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755584
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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