A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6783169



Internal ID9841164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:3215791..3216211hg38UCSC Ensembl
Outerchr10:3257983..3258403hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2730995, esv2731306
Supporting Variants
SamplesSSM068
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)essv6783169
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