A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518273



Internal ID20891634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48775301..48786000hg38UCSC Ensembl
chr18:46301672..46312371hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042090
Samples
Known GenesCTIF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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