A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522682



Internal ID20896043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50737940..50739277hg38UCSC Ensembl
chr18:48264310..48265647hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381338
hg191338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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