A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525023



Internal ID20898384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74478638..74483097hg38UCSC Ensembl
chr18:72145873..72150332hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg384460
hg194460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525023
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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