A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525748



Internal ID20899109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68030263..68301855hg38UCSC Ensembl
chr18:65697500..65969092hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38271593
hg19271593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525748
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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