A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1715n100



Internal ID22787802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79845361..79883551hg38UCSC Ensembl
chr13:80419496..80457686hg19UCSC Ensembl
chr13:79317497..79355687hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3838191
hg1938191
hg1838191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048990, nsv1044254
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)dgv1715n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer