A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1291n54



Internal ID22769186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80453946..80454751hg38UCSC Ensembl
chr10:82213702..82214507hg19UCSC Ensembl
chr10:82203682..82204487hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38806
hg19806
hg18806
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551639, nsv551638
Samples
Known GenesTSPAN14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1291n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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