A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426917



Internal ID21084470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143297334..143319444hg38UCSC Ensembl
chr8:144379504..144401614hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3822111
hg1922111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165463
Samples
Known GenesTOP1MT, ZNF696
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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