A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4017681



Internal ID22079312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89487306..89497867hg38UCSC Ensembl
Outerchr3:89475943..89503594hg38UCSC Ensembl
Innerchr3:89536456..89547017hg19UCSC Ensembl
Outerchr3:89525093..89552744hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3827652
hg1927652
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156001
Supporting Variants
Samples
Known GenesEPHA3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4017681
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