A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758861



Internal ID20534721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35226715..35226715hg38UCSC Ensembl
chr20:33814518..33814518hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758861
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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