A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3344n100



Internal ID22789431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42460509..42478430hg38UCSC Ensembl
chr18:40040474..40058395hg19UCSC Ensembl
chr18:38294472..38312393hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3817922
hg1917922
hg1817922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062292, nsv1056192, nsv1059650, nsv1055622
Samples
Known GenesLINC00907
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3344n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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