A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519211



Internal ID20892572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58453226..58454678hg38UCSC Ensembl
chr18:56120458..56121910hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg381453
hg191453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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