A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266175



Internal ID20475393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208128720..208128720hg38UCSC Ensembl
chr2:208993444..208993444hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753481
Supporting Variants
Samples
Known GenesCRYGC, LOC100507443
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266175
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