A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744227



Internal ID18695822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134002879..134267235hg38UCSC Ensembl
Innerchr4:134924034..135188390hg19UCSC Ensembl
Innerchr4:135143484..135407840hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38264357
hg19264357
hg18264357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020818
Supporting Variants
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)nssv3744227
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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