A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004467



Internal ID22066098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112078848..112092083hg38UCSC Ensembl
Outerchr10:112077880..112094141hg38UCSC Ensembl
Innerchr10:113838606..113851841hg19UCSC Ensembl
Outerchr10:113837638..113853899hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3816262
hg1916262
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154654
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004467
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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