A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6895913



Internal ID10289804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:113497173..113503253hg38UCSC Ensembl
Outerchr1:114039795..114045875hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg386081
hg196081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716440
Supporting Variants
SamplesSSM099
Known GenesMAGI3
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)essv6895913
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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