A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518363



Internal ID20891724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55557569..55569036hg38UCSC Ensembl
chr18:53224800..53236267hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3811468
hg1911468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042503
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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