A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533246



Internal ID20906607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77526706..77527414hg38UCSC Ensembl
chr18:75238662..75239370hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533246
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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