A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102435



Internal ID22011670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47255718..47255718hg38UCSC Ensembl
chr20:45884462..45884462hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623697
Samples
Known GenesZMYND8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102435
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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