A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6896198



Internal ID9665964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26709949..26713222hg38UCSC Ensembl
Outerchr10:26998878..27002151hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383274
hg193274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734406
Supporting Variants
SamplesSSM012
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)essv6896198
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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