A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524211



Internal ID20897572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69821963..69822333hg38UCSC Ensembl
chr18:67489199..67489569hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043662
Samples
Known GenesDOK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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