A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531158



Internal ID20904519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:527107..530491hg38UCSC Ensembl
chr20:507751..511135hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383385
hg193385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068217
Samples
Known GenesCSNK2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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