A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2813n100



Internal ID20154429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22412835..22699409hg38UCSC Ensembl
chr16:22424156..22710730hg19UCSC Ensembl
chr16:22331657..22618231hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38286575
hg19286575
hg18286575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039921, nsv1044056
Samples
Known GenesLOC100190986, LOC653786, NPIPB5, RRN3P3, SMG1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2813n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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