A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426508



Internal ID21084061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81517501..81530600hg38UCSC Ensembl
chr8:82429736..82442835hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3813100
hg1913100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228244
Samples
Known GenesFABP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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