A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101864



Internal ID22011097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40823776..40823776hg38UCSC Ensembl
chr20:39452416..39452416hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101864
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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