A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7249n100



Internal ID22793336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83631699..83846576hg38UCSC Ensembl
chr8:84543934..84758811hg19UCSC Ensembl
chr8:84706489..84921366hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38214878
hg19214878
hg18214878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018202, nsv1028924
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)dgv7249n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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