A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015663



Internal ID22077294
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156238
Supporting Variants
Samples
Known GenesTMEM184C
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015663
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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