A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156248



Internal ID22086753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156834239..156846147hg38UCSC Ensembl
Outerchr4:156831751..156853588hg38UCSC Ensembl
Innerchr4:157755391..157767299hg19UCSC Ensembl
Outerchr4:157752903..157774740hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3821838
hg1921838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015724
Samples
Known GenesPDGFC
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156248
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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