A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529031



Internal ID20902392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38988093..39014212hg38UCSC Ensembl
chr18:36568057..36594176hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3826120
hg1926120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529031
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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