A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1338n54



Internal ID20134762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90322493..90839066hg38UCSC Ensembl
chr10:92082250..92598823hg19UCSC Ensembl
chr10:92072230..92588803hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38516574
hg19516574
hg18516574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551879, nsv551881, nsv551882, nsv551880
SamplesNINDS_59
Known GenesHTR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1338n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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