A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6869409



Internal ID10008283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64340987..64341345hg38UCSC Ensembl
Outerchr15:64633186..64633544hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749781
Supporting Variants
SamplesSSM011
Known GenesCSNK1G1
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)essv6869409
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