A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518020



Internal ID20891381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12292364..12292686hg38UCSC Ensembl
chr18:12292363..12292685hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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