A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2729n100



Internal ID20154345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11483511..11548386hg38UCSC Ensembl
chr16:11577367..11642242hg19UCSC Ensembl
chr16:11484868..11549743hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3864876
hg1964876
hg1864876
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044993, nsv1035174, nsv1035771, nsv1048952
Samples
Known GenesLITAF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2729n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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