A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518845



Internal ID20892206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59938014..59946706hg38UCSC Ensembl
chr18:57605246..57613938hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg388693
hg198693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518845
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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