A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1320n54



Internal ID18993496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86653016..86668546hg38UCSC Ensembl
chr10:88412773..88428303hg19UCSC Ensembl
chr10:88402753..88418283hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3815531
hg1915531
hg1815531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551789, nsv551784
Samples
Known GenesLDB3, OPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1320n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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