A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1335n54



Internal ID22769230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89180601..89204638hg38UCSC Ensembl
chr10:90940358..90964395hg19UCSC Ensembl
chr10:90930338..90954375hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3824038
hg1924038
hg1824038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551868, nsv551857, nsv551867, nsv551862, nsv551873, nsv551870, nsv551848, nsv551872, nsv551856
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1335n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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