A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12929n54



Internal ID20146353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133090975..133155959hg38UCSC Ensembl
chr9:135966362..136031346hg19UCSC Ensembl
chr9:134956183..135021167hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3864985
hg1964985
hg1864985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615609, nsv615610, nsv615607
SamplesNINDS_66
Known GenesGBGT1, RALGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12929n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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