A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7109n100



Internal ID22793196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16086558..16167255hg38UCSC Ensembl
chr8:15944067..16024764hg19UCSC Ensembl
chr8:15988438..16069135hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3880698
hg1980698
hg1880698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022644, nsv1025124, nsv1025560, nsv1019412, nsv1032023, nsv1016636, nsv1029307
Samples
Known GenesMSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7109n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss56
Observed Complex0
Frequencyn/a


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