A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2996n100



Internal ID22789083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68144536..68207851hg38UCSC Ensembl
chr16:68178439..68241754hg19UCSC Ensembl
chr16:66735940..66799255hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3863316
hg1963316
hg1863316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064080, nsv1058050
Samples
Known GenesNFATC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2996n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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