A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3397n100



Internal ID22789484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70458582..70499331hg38UCSC Ensembl
chr18:68125818..68166567hg19UCSC Ensembl
chr18:66276798..66317547hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3840750
hg1940750
hg1840750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064740, nsv1061526, nsv1064014
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3397n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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