A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518932



Internal ID20892293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:80227796..80262675hg38UCSC Ensembl
chr18:77985679..78017154hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3834880
hg1931476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197981
Samples
Known GenesPARD6G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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