A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532600



Internal ID20905961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66944575..67055359hg38UCSC Ensembl
chr18:64611812..64722596hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38110785
hg19110785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532600
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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