A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757084



Internal ID20532944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62105763..62105763hg38UCSC Ensembl
chr20:60680819..60680819hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757084
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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