A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7141n100



Internal ID19017509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24436486..24511427hg38UCSC Ensembl
chr8:24293999..24368940hg19UCSC Ensembl
chr8:24349944..24424830hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3874942
hg1974942
hg1874887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022221, nsv1032200
Samples
Known GenesADAM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7141n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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