A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7674n100



Internal ID20159290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69485135..69505349hg38UCSC Ensembl
chr9:72100051..72120265hg19UCSC Ensembl
chr9:71289871..71310085hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3820215
hg1920215
hg1820215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043227, nsv1052038, nsv1048073, nsv1038261
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7674n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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