A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156238



Internal ID22086743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:147595618..147614485hg38UCSC Ensembl
Outerchr4:147594492..147619655hg38UCSC Ensembl
Innerchr4:148516769..148535636hg19UCSC Ensembl
Outerchr4:148515644..148540806hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3825164
hg1925163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015663
Samples
Known GenesTMEM184C
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156238
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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