A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6913922



Internal ID9677487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:44422776..44423167hg38UCSC Ensembl
Outerchr21:45842659..45843050hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723638, esv2723655
Supporting Variants
SamplesSSM015
Known GenesTRPM2
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)essv6913922
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