A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6866849



Internal ID10263645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131110805..131114466hg38UCSC Ensembl
Outerchr10:132909068..132912729hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383662
hg193662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743528
Supporting Variants
SamplesSSM089
Known GenesTCERG1L
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)essv6866849
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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