A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6863886



Internal ID9663366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132352049..132352612hg38UCSC Ensembl
Outerchr10:134165553..134166116hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743654
Supporting Variants
SamplesSSM011
Known GenesLRRC27
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)essv6863886
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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