A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000838



Internal ID21910181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33497652..33497705hg38UCSC Ensembl
chr8:33355170..33355223hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565020
Samples
Known GenesMAK16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000838
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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