A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523766



Internal ID20897127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23134901..23138100hg38UCSC Ensembl
chr18:20714865..20718064hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179145
Samples
Known GenesCABLES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523766
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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