A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2724n100



Internal ID22788811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8084931..8173955hg38UCSC Ensembl
chr16:8134933..8223957hg19UCSC Ensembl
chr16:8074934..8163958hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3889025
hg1989025
hg1889025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052759, nsv1046039
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)dgv2724n100
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