A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283414



Internal ID20492632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85158980..85158980hg38UCSC Ensembl
chr6:85868698..85868698hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765925
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283414
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