A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767634



Internal ID20543494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59442193..59442193hg38UCSC Ensembl
chr20:58017248..58017248hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767634
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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