A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12623n54



Internal ID22780518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28049520..28051193hg38UCSC Ensembl
chr9:28049518..28051191hg19UCSC Ensembl
chr9:28039518..28041191hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381674
hg191674
hg181674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613959, nsv613958, nsv613957, nsv613962, nsv613961
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12623n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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