A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014239



Internal ID22075870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39702789..39711713hg38UCSC Ensembl
Outerchr4:39702577..39711868hg38UCSC Ensembl
Innerchr4:39704409..39713333hg19UCSC Ensembl
Outerchr4:39704197..39713488hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg389292
hg199292
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156147
Supporting Variants
Samples
Known GenesUBE2K
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014239
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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