A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751464



Internal ID20527324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36663044..36663044hg38UCSC Ensembl
chr20:35291447..35291447hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279010
Samples
Known GenesNDRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751464
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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