A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016559



Internal ID18759094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134002879..134257197hg38UCSC Ensembl
Innerchr4:134924034..135178352hg19UCSC Ensembl
Innerchr4:135143484..135397802hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38254319
hg19254319
hg18254319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5397n100
Supporting Variantsnssv3743112
Samples
Known GenesPABPC4L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016559
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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