A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010922



Internal ID21920265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90224761..90234720hg38UCSC Ensembl
chr8:91236989..91246948hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg389960
hg199960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578835
Samples
Known GenesLINC00534
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010922
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