A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3262n54



Internal ID22771157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77697539..77698481hg38UCSC Ensembl
chr13:78271674..78272616hg19UCSC Ensembl
chr13:77169675..77170617hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38943
hg19943
hg18943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562386, nsv562378, nsv562379, nsv562380, nsv562385, nsv562381, nsv562382
Samples
Known GenesMIR3665, SLAIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3262n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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