A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3338n100



Internal ID20154954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39636758..39693083hg38UCSC Ensembl
chr18:37216722..37273047hg19UCSC Ensembl
chr18:35470720..35527045hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3856326
hg1956326
hg1856326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063581, nsv1064182
Samples
Known GenesLINC00669, MIR5583-1, MIR5583-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3338n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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