A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910007



Internal ID7447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10441725..10441816hg38UCSC Ensembl
chr2:10581851..10581942hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452274
Supporting Variants
Samples
Known GenesODC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910007
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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