A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065396



Internal ID21974629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:511333..511333hg38UCSC Ensembl
chr7:550970..550970hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559906
Samples
Known GenesPDGFA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065396
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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