A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6923979



Internal ID9686627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14939255..15021366hg38UCSC Ensembl
Outerchr10:14981254..15063365hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3882112
hg1982112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733506
Supporting Variants
SamplesSSM018
Known GenesDCLRE1C, MEIG1
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)essv6923979
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