A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518453



Internal ID20891814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74267321..74267796hg38UCSC Ensembl
chr18:71934556..71935031hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043692
Samples
Known GenesCYB5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518453
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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