A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016487



Internal ID18759022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134002879..134259039hg38UCSC Ensembl
Innerchr4:134924034..135180194hg19UCSC Ensembl
Innerchr4:135143484..135399644hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38256161
hg19256161
hg18256161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5397n100
Supporting Variantsnssv3743113
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)nsv1016487
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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