A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760277



Internal ID20536137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54188949..54188949hg38UCSC Ensembl
chr20:52805488..52805488hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760277
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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