A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118047



Internal ID21301313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22165218..22167131hg38UCSC Ensembl
Innerchr18:19745179..19747092hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381914
hg191914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099535
Samplessample98
Known GenesGATA6-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118047
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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