A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12932n54



Internal ID22780827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133255963..133257183hg38UCSC Ensembl
chr9:136131350..136132570hg19UCSC Ensembl
chr9:135121171..135122391hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381221
hg191221
hg181221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615620, nsv615618, nsv615619
Samples
Known GenesABO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12932n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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