A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1598n100



Internal ID22787685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18471488..18687960hg38UCSC Ensembl
chr13:19045628..19262100hg19UCSC Ensembl
chr13:17943628..18160100hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38216473
hg19216473
hg18216473
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035799, nsv1043433
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)dgv1598n100
Frequency
Sample Size11257
Observed Gain21
Observed Loss2
Observed Complex0
Frequencyn/a


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