A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072359



Internal ID21981592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168118586..168118586hg38UCSC Ensembl
chr5:167545591..167545591hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561447
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072359
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