A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737064



Internal ID20513021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34889380..34889513hg38UCSC Ensembl
chr20:33477183..33477316hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270471
Samples
Known GenesACSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737064
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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