A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1739n100



Internal ID22787826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105633807..105695924hg38UCSC Ensembl
chr13:106286156..106348273hg19UCSC Ensembl
chr13:105084157..105146274hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3862118
hg1962118
hg1862118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050042, nsv1050333
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1739n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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