A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1395n54



Internal ID22769290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112353831..112356817hg38UCSC Ensembl
chr10:114113589..114116575hg19UCSC Ensembl
chr10:114103579..114106565hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382987
hg192987
hg182987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552177, nsv552176, nsv552178
Samples
Known GenesGUCY2GP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1395n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss324
Observed Complex0
Frequencyn/a


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