A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040246



Internal ID21949589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56600358..56600424hg38UCSC Ensembl
chr18:54267589..54267655hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040246
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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