A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6806185



Internal ID9861355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103337733..103338119hg38UCSC Ensembl
Outerchr10:105097490..105097876hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2740273
Supporting Variants
SamplesSSM074
Known GenesPCGF6
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)essv6806185
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