A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735367



Internal ID20511309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58828821..58828927hg38UCSC Ensembl
chr20:57403876..57403982hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276045
Samples
Known GenesGNAS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735367
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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