A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110103



Internal ID22019336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51651336..51651336hg38UCSC Ensembl
chr20:50267875..50267875hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621835
Samples
Known GenesATP9A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110103
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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