A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3375n100



Internal ID22789462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60797118..60827446hg38UCSC Ensembl
chr18:58464351..58494679hg19UCSC Ensembl
chr18:56615331..56645659hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3830329
hg1930329
hg1830329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062506, nsv1067454, nsv1065076
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)dgv3375n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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