A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055615



Internal ID21964848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58828926..58828999hg38UCSC Ensembl
chr20:57403981..57404054hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630077
Samples
Known GenesGNAS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055615
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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