A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067357



Internal ID21976590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154827730..154827730hg38UCSC Ensembl
chr7:154619440..154619440hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570353
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067357
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