A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9216n54



Internal ID22777111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109433476..109434327hg38UCSC Ensembl
chr4:110354632..110355483hg19UCSC Ensembl
chr4:110574081..110574932hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38852
hg19852
hg18852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595139, nsv595141, nsv595140, nsv595134, nsv595135, nsv595138
Samples
Known GenesSEC24B, SEC24B-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9216n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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