A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6905047



Internal ID9670768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:46464681..46465962hg38UCSC Ensembl
Outerchr13:47038816..47040097hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381282
hg191282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747362
Supporting Variants
SamplesSSM013
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)essv6905047
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