A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275102



Internal ID20484320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154956338..154956338hg38UCSC Ensembl
chr6:155277472..155277472hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759067
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275102
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