A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6897402



Internal ID9944894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26710012..26713226hg38UCSC Ensembl
Outerchr10:26998941..27002155hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383215
hg193215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734406
Supporting Variants
SamplesSSM099
Known GenesPDSS1
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)essv6897402
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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