A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111875



Internal ID21295141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3602778..3637381hg38UCSC Ensembl
Innerchr18:3602776..3637380hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3834604
hg1934605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100130
Samplessample274
Known GenesDLGAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111875
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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