A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527495



Internal ID20900856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66820998..66943610hg38UCSC Ensembl
chr18:64488235..64610847hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38122613
hg19122613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527495
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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