A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7397n223



Internal ID22810365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81520601..81526200hg38UCSC Ensembl
chr8:82432836..82438435hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6418601, nsv6428722
Samples
Known GenesFABP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7397n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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