A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105971



Internal ID22015204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50941394..50941394hg38UCSC Ensembl
chr20:49557931..49557931hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621709
Samples
Known GenesDPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105971
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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