A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3339n100



Internal ID22789426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40237274..40269920hg38UCSC Ensembl
chr18:37817238..37849884hg19UCSC Ensembl
chr18:36071236..36103882hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3832647
hg1932647
hg1832647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066669, nsv1061832
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)dgv3339n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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