A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6830999



Internal ID10231380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26574140..26627797hg38UCSC Ensembl
Outerchr10:26863069..26916726hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3853658
hg1953658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734384
Supporting Variants
SamplesSSM081
Known GenesLINC00264
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)essv6830999
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