A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042233



Internal ID19131452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105305766..105333955hg38UCSC Ensembl
Innerchr13:105958117..105986306hg19UCSC Ensembl
Innerchr13:104756118..104784307hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3828190
hg1928190
hg1828190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525559
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042233
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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