A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420357



Internal ID21077910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64795701..64801500hg38UCSC Ensembl
chr8:65708258..65714057hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233089
Samples
Known GenesCYP7B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420357
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