A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736402



Internal ID20512351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32739569..32740241hg38UCSC Ensembl
chr20:31327376..31328048hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287490
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736402
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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