A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6862935



Internal ID9910861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:89325105..89325251hg38UCSC Ensembl
Outerchr15:89868336..89868482hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750000, esv2750001, esv2749999
Supporting Variants
SamplesSSM088
Known GenesPOLG
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)essv6862935
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