A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051370



Internal ID20618410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113099171..113102477hg38UCSC Ensembl
chr1:113641793..113645099hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg383307
hg193307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320114
Supporting Variants
Samples
Known GenesLRIG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051370
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