A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516831



Internal ID20890192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70427767..70429155hg38UCSC Ensembl
chr18:68095003..68096391hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg381389
hg191389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516831
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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