A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427667



Internal ID21085220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81511051..81631204hg38UCSC Ensembl
chr8:82423286..82543439hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38120154
hg19120154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228831
Samples
Known GenesFABP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer