A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1615n100



Internal ID20153231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:22930769..24362849hg38UCSC Ensembl
chr13:23504908..24936987hg19UCSC Ensembl
chr13:22402908..23834987hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381432081
hg191432080
hg181432080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044362, nsv1051907, nsv1053678, nsv1043043, nsv1041938
Samples
Known GenesANKRD20A19P, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1615n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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