A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3381n100



Internal ID20154997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66413169..66674437hg38UCSC Ensembl
chr18:64080406..64341674hg19UCSC Ensembl
chr18:62231386..62492654hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38261269
hg19261269
hg18261269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058280, nsv1062945, nsv1058812
Samples
Known GenesCDH19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3381n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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