A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9492n54



Internal ID22777387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:474296..474989hg38UCSC Ensembl
chr5:474411..475104hg19UCSC Ensembl
chr5:527411..528104hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38694
hg19694
hg18694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596690, nsv596692
Samples
Known GenesSLC9A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9492n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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