A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11063n54



Internal ID20144487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167941569..168149659hg38UCSC Ensembl
chr6:168342249..168550339hg19UCSC Ensembl
chr6:168085098..168293188hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38208091
hg19208091
hg18208091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605393, nsv605398, nsv605399, nsv605396, nsv605409, nsv605397, nsv605441, nsv605400
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11063n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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