A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546343



Internal ID20919561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58864147..58868344hg38UCSC Ensembl
chr20:57439202..57443399hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg384198
hg194198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069130
Samples
Known GenesGNAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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