A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767408



Internal ID20543268
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 StatusM
Merged Variants
Supporting Variantsnssv16273436
Samples
Known GenesDST
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767408
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