A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293155



Internal ID20502373
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 StatusS
Merged Variantsnsv4755584
Supporting Variants
Samples
Known GenesARHGAP40
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293155
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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