A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525068



Internal ID20898429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48173869..48174751hg38UCSC Ensembl
chr18:45700240..45701122hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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