A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763140



Internal ID20539000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:537523..537523hg38UCSC Ensembl
chr7:577160..577160hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763140
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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