A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021393



Internal ID18763927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134002879..134264464hg38UCSC Ensembl
Innerchr4:134924034..135185619hg19UCSC Ensembl
Innerchr4:135143484..135405069hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38261586
hg19261586
hg18261586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5397n100
Supporting Variantsnssv3639539, nssv3639544, nssv3744224, nssv3744222, nssv3639542, nssv3743114, nssv3744223, nssv3639545, nssv3639541, nssv3639540, nssv3744225, nssv3639543
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)nsv1021393
Frequency
Sample Size29084
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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