A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047580



Internal ID21956814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58830144..58830246hg38UCSC Ensembl
chr20:57405199..57405301hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619430
Samples
Known GenesGNAS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047580
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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