A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7202n100



Internal ID22793289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:45935900..46865275hg38UCSC Ensembl
chr8:46847522..47776897hg19UCSC Ensembl
chr8:46966687..47896062hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38929376
hg19929376
hg18929376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031161, nsv1025020, nsv1018479, nsv1032451, nsv1030943, nsv1031244
Samples
Known GenesLINC00293
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7202n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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