A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292610



Internal ID20501828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109199328..109199764hg38UCSC Ensembl
chr2:109815784..109816220hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742316
Supporting Variants
Samples
Known GenesSH3RF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292610
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer