A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156147



Internal ID22086652
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 TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014238, nssv4014239
Samples
Known GenesUBE2K
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156147
Frequency
Sample Size131
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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