A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3317n54



Internal ID22771212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91348005..91349218hg38UCSC Ensembl
chr13:92000259..92001472hg19UCSC Ensembl
chr13:90798260..90799473hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381214
hg191214
hg181214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562712, nsv562709, nsv562713
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3317n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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