A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3386n100



Internal ID22789473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67588657..68009670hg38UCSC Ensembl
chr18:65255894..65676907hg19UCSC Ensembl
chr18:63406874..63827887hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38421014
hg19421014
hg18421014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063370, nsv1066205
Samples
Known GenesLOC643542
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3386n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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