A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751398



Internal ID20527258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20458707..20458707hg38UCSC Ensembl
chr20:20439351..20439351hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278832
Samples
Known GenesRALGAPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751398
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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