A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014244



Internal ID22075875
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156152
Supporting Variants
Samples
Known GenesGRXCR1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014244
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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