A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536188



Internal ID20909543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43631036..43692880hg38UCSC Ensembl
chr20:42259676..42321520hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3861845
hg1961845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067782
Samples
Known GenesIFT52, MYBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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