A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015896



Internal ID22077527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138057321..138082564hg38UCSC Ensembl
Outerchr3:138053148..138086356hg38UCSC Ensembl
Innerchr3:137776163..137801406hg19UCSC Ensembl
Outerchr3:137771990..137805198hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3833209
hg1933209
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156020
Supporting Variants
Samples
Known GenesDZIP1L
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015896
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