A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528928



Internal ID20902289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38055712..38077424hg38UCSC Ensembl
chr18:35635676..35657388hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3821713
hg1921713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528928
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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