A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1705n100



Internal ID22787792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68659887..68694098hg38UCSC Ensembl
chr13:69234019..69268230hg19UCSC Ensembl
chr13:68132020..68166231hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3834212
hg1934212
hg1834212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047512, nsv1051459, nsv1043903
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)dgv1705n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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