A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420662



Internal ID21078215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10829849..11153243hg38UCSC Ensembl
chr8:10687359..11010753hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38323395
hg19323395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236990
Samples
Known GenesMIR598, PINX1, XKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420662
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