A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274368



Internal ID20483586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157039662..157039662hg38UCSC Ensembl
chr6:157360796..157360796hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760822
Supporting Variants
Samples
Known GenesARID1B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274368
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