A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3337n100



Internal ID22789424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39360269..39456067hg38UCSC Ensembl
chr18:36940233..37036031hg19UCSC Ensembl
chr18:35194231..35290029hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3895799
hg1995799
hg1895799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063320, nsv1059761
Samples
Known GenesLINC00669
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3337n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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