A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534197



Internal ID20907558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61728801..61800800hg38UCSC Ensembl
chr18:59396034..59468033hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3872000
hg1972000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043310
Samples
Known GenesLOC100996669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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