A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10918n54



Internal ID20144342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118401426..118792154hg38UCSC Ensembl
chr6:118722589..119113317hg19UCSC Ensembl
chr6:118829282..119220010hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38390729
hg19390729
hg18390729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604556, nsv604559
Samples
Known GenesBRD7P3, CEP85L, LOC100287632, PLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10918n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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