A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103753



Internal ID22012986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50258483..50258483hg38UCSC Ensembl
chr20:48875020..48875020hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103753
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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