A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7673n100



Internal ID20159289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69482727..69512782hg38UCSC Ensembl
chr9:72097643..72127698hg19UCSC Ensembl
chr9:71287463..71317518hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3830056
hg1930056
hg1830056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044064, nsv1051568, nsv1041391
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)dgv7673n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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