A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113726



Internal ID21296992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:30925254..30937698hg38UCSC Ensembl
Innerchr4:30926876..30939320hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3812445
hg1912445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094856
Samplessample383
Known GenesPCDH7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113726
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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