A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525240



Internal ID20898601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49516624..49520609hg38UCSC Ensembl
chr18:47042994..47046979hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg383986
hg193986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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