A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520903



Internal ID20894264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48563577..48608434hg38UCSC Ensembl
chr18:46089948..46134805hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3844858
hg1944858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194969
Samples
Known GenesCTIF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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