A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1698n100



Internal ID22787785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:64683335..64745204hg38UCSC Ensembl
chr13:65257467..65319336hg19UCSC Ensembl
chr13:64155468..64217337hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3861870
hg1961870
hg1861870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044887, nsv1051377
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)dgv1698n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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