A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10e198



Internal ID22757742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26991709..26992226hg38UCSC Ensembl
chr18:24571673..24572190hg19UCSC Ensembl
chr18:22825671..22826188hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38518
hg19518
hg18518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2656301, esv2656280, esv2656222, esv2656161, esv2656088, esv2656133, esv2656374
Samples2333 [30], 2244 [61], 2342 [37], 2290 [64], 2308 [7], 2345 [40], 2360 [53]
Known GenesCHST9
MethodMerging
AnalysisCalls merged from CNV Partition and PennCV algorithms
PlatformMerging
Comments
ReferenceChia_et_al_2012
Pubmed ID23635498
Accession Number(s)dgv10e198
Frequency
Sample Size64
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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