A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533384



Internal ID20906745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10379249..10533407hg38UCSC Ensembl
chr18:10379246..10533404hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38154159
hg19154159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178889
Samples
Known GenesAPCDD1, NAPG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533384
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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