A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1728n100



Internal ID22787815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90195324..90403358hg38UCSC Ensembl
chr13:90847578..91055612hg19UCSC Ensembl
chr13:89645579..89853613hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38208035
hg19208035
hg18208035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045825, nsv1046364
Samples
Known GenesMIR622
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1728n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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