A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028039



Internal ID18770570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134003215..134267621hg38UCSC Ensembl
Innerchr4:134924370..135188776hg19UCSC Ensembl
Innerchr4:135143820..135408226hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38264407
hg19264407
hg18264407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5397n100
Supporting Variantsnssv3639554
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)nsv1028039
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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