A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558250



Internal ID21882605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158310752..158310752hg38UCSC Ensembl
chr7:158103444..158103444hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080415
Supporting Variants
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558250
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