A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1322n54



Internal ID22769217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86654460..86662305hg38UCSC Ensembl
chr10:88414217..88422062hg19UCSC Ensembl
chr10:88404197..88412042hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg387846
hg197846
hg187846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551788, nsv551786
Samples
Known GenesOPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1322n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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