A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522361



Internal ID20895722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58792787..58796991hg38UCSC Ensembl
chr18:56460019..56464223hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg384205
hg194205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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