A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1351n54



Internal ID20134775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92689478..92690472hg38UCSC Ensembl
chr10:94449235..94450229hg19UCSC Ensembl
chr10:94439215..94440209hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38995
hg19995
hg18995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551932, nsv551927, nsv551931
Samples
Known GenesHHEX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1351n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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