A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273436



Internal ID20482654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56864511..56864511hg38UCSC Ensembl
chr6:56729309..56729309hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767408
Supporting Variants
Samples
Known GenesDST
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273436
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