A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624625



Internal ID21572930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148869338..148869338hg38UCSC Ensembl
chr7:148566430..148566430hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152983
SamplesNA19239
Known GenesEZH2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624625
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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