A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8827n54



Internal ID22776722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195270602..195271166hg38UCSC Ensembl
chr3:194991331..194991895hg19UCSC Ensembl
chr3:196472620..196473184hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38565
hg19565
hg18565
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592986, nsv592989, nsv592985
Samples
Known GenesXXYLT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8827n54
Frequency
Sample Size17421
Observed Gain17
Observed Loss14
Observed Complex0
Frequencyn/a


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