A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10624n54



Internal ID20144048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35489619..35497706hg38UCSC Ensembl
chr6:35457396..35465483hg19UCSC Ensembl
chr6:35565374..35573461hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg388088
hg198088
hg188088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602913, nsv602911
Samples
Known GenesTEAD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10624n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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