A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522432



Internal ID20895793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:1348499..2307331hg38UCSC Ensembl
chr18:1348500..2307330hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38958833
hg19958831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184674
Samples
Known GenesLINC00470
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522432
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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