A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6896298



Internal ID9665955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:44866323..44866716hg38UCSC Ensembl
Outerchr10:45361771..45362164hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736072
Supporting Variants
SamplesSSM012
Known GenesTMEM72-AS1
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)essv6896298
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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