A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034385



Internal ID19123607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134002879..134267621hg38UCSC Ensembl
Innerchr4:134924034..135188776hg19UCSC Ensembl
Innerchr4:135143484..135408226hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38264743
hg19264743
hg18264743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5397n100
Supporting Variantsnssv3744229, nssv3744230, nssv3639552, nssv3639553, nssv3744231
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)nsv1034385
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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