A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18076332



Internal ID20643372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1288419..1310461hg38UCSC Ensembl
chr2:1292191..1314233hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3822043
hg1922043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317731
Supporting Variants
Samples
Known GenesSNTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18076332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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