A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521652



Internal ID20895013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63299601..63402400hg38UCSC Ensembl
chr18:60966834..61069633hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38102800
hg19102800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190782
Samples
Known GenesBCL2, KDSR, VPS4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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