A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7672n100



Internal ID20159288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69482727..69505349hg38UCSC Ensembl
chr9:72097643..72120265hg19UCSC Ensembl
chr9:71287463..71310085hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3822623
hg1922623
hg1822623
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054541, nsv1038600, nsv1045089, nsv1050573
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)dgv7672n100
Frequency
Sample Size29084
Observed Gain45
Observed Loss38
Observed Complex0
Frequencyn/a


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