A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156152



Internal ID22086657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42857623..43109077hg38UCSC Ensembl
Outerchr4:42855811..43111382hg38UCSC Ensembl
Innerchr4:42859640..43111094hg19UCSC Ensembl
Outerchr4:42857828..43113399hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38255572
hg19255572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014244
Samples
Known GenesGRXCR1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156152
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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