A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415646



Internal ID21073199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11500355..11528198hg38UCSC Ensembl
chr8:11357864..11385707hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3827844
hg1927844
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233736
Samples
Known GenesBLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415646
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