A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521348



Internal ID20894709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32791301..32799600hg38UCSC Ensembl
chr18:30371264..30379563hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521348
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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