A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742079



Internal ID20518058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148810713..148810777hg38UCSC Ensembl
chr7:148507805..148507869hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263474
Samples
Known GenesEZH2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742079
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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