A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7161n100



Internal ID22793248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36559791..36624593hg38UCSC Ensembl
chr8:36417309..36482111hg19UCSC Ensembl
chr8:36536467..36601269hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3864803
hg1964803
hg1864803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023001, nsv1016306
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)dgv7161n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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