A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756101



Internal ID20531961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63288315..63288315hg38UCSC Ensembl
chr20:61919667..61919667hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272243
Samples
Known GenesARFGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756101
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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