A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8828n54



Internal ID22776723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195270602..195274367hg38UCSC Ensembl
chr3:194991331..194995096hg19UCSC Ensembl
chr3:196472620..196476385hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg383766
hg193766
hg183766
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592988, nsv592987
Samples
Known GenesXXYLT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8828n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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