A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11068n54



Internal ID22778963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168316995..168317914hg38UCSC Ensembl
chr6:168717675..168718594hg19UCSC Ensembl
chr6:168460524..168461443hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38920
hg19920
hg18920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605469, nsv605471
Samples
Known GenesDACT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11068n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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