A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998083



Internal ID6734023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89323531..89323610hg38UCSC Ensembl
chr16:89389939..89390018hg19UCSC Ensembl
chr16:87917440..87917519hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3880
hg1980
hg1880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3571917
SamplesHuRef
Known GenesANKRD11, LOC100287036
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998083
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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