A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427276



Internal ID21084829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52447893..52601794hg38UCSC Ensembl
chr8:53360453..53514354hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38153902
hg19153902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7343n223
Supporting Variantsnssv18234362
Samples
Known GenesFAM150A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427276
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