A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156003



Internal ID22086508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89838281..89842618hg38UCSC Ensembl
Outerchr3:89830994..89848673hg38UCSC Ensembl
Innerchr3:89887431..89891768hg19UCSC Ensembl
Outerchr3:89880144..89897823hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3817680
hg1917680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017684
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156003
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