A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10311n54



Internal ID22778206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18698911..19116208hg38UCSC Ensembl
chr6:18699142..19116439hg19UCSC Ensembl
chr6:18807121..19224418hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38417298
hg19417298
hg18417298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601056, nsv601055
Samples1780862347_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10311n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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