A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521523



Internal ID20894884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69400201..69402900hg38UCSC Ensembl
chr18:67067437..67070136hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197629
Samples
Known GenesDOK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521523
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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