A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603578



Internal ID21795625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10092256..10136932hg38UCSC Ensembl
chr16:10186113..10230789hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3844677
hg1944677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031376
Supporting Variants
Samples
Known GenesGRIN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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