A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1339n54



Internal ID22769234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90697976..90705170hg38UCSC Ensembl
chr10:92457733..92464927hg19UCSC Ensembl
chr10:92447713..92454907hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg387195
hg197195
hg187195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551886, nsv551884, nsv551885
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1339n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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