A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3392n100



Internal ID22789479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68228789..68511817hg38UCSC Ensembl
chr18:65896026..66179054hg19UCSC Ensembl
chr18:64047006..64330034hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38283029
hg19283029
hg18283029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060990, nsv1067400
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)dgv3392n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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