A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12744n54



Internal ID20146168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69485135..69519460hg38UCSC Ensembl
chr9:72100051..72134376hg19UCSC Ensembl
chr9:71289871..71324196hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3834326
hg1934326
hg1834326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614573, nsv614578
SamplesHGDP00594
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12744n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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