A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6901817



Internal ID10011935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:46402293..46419470hg38UCSC Ensembl
Outerchr16:46436205..46453382hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3817178
hg1917178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714419, esv2714399, esv2714405, esv2714402, esv2714391, esv2714384, esv2714397, esv2714412, esv2714408
Supporting Variants
SamplesSSM012
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6901817
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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