A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521762



Internal ID20895123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34324973..34345270hg38UCSC Ensembl
chr18:31904937..31925234hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3820298
hg1920298
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521762
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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