A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4913n54



Internal ID20138337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13200753..13202426hg38UCSC Ensembl
chr16:13294610..13296283hg19UCSC Ensembl
chr16:13202111..13203784hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381674
hg191674
hg181674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571494, nsv571487, nsv571492, nsv571496, nsv571498, nsv571495, nsv571499, nsv571485, nsv571489, nsv571486, nsv571500, nsv571501, nsv571488, nsv571497, nsv571502
Samples
Known GenesSHISA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4913n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss201
Observed Complex0
Frequencyn/a


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