A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757622



Internal ID20533482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33147376..33147376hg38UCSC Ensembl
chr20:31735182..31735182hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757622
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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