A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528882



Internal ID20902243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78670408..78695707hg38UCSC Ensembl
chr18:76430408..76455707hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3825300
hg1925300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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