A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425019



Internal ID21082572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27507322..27517479hg38UCSC Ensembl
chr8:27364839..27374996hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3810158
hg1910158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236901
Samples
Known GenesEPHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425019
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