A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2699n100



Internal ID22788786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5376302..5596284hg38UCSC Ensembl
chr16:5426303..5646285hg19UCSC Ensembl
chr16:5366304..5586286hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38219983
hg19219983
hg18219983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040920, nsv1037742
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)dgv2699n100
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