A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755109



Internal ID20530969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37914394..37914394hg38UCSC Ensembl
chr20:36542796..36542796hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281439
Samples
Known GenesVSTM2L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755109
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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