A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553185



Internal ID20926294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49125555..49127877hg38UCSC Ensembl
chr20:47742092..47744414hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382323
hg192323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068960
Samples
Known GenesSTAU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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