A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6891086



Internal ID10285459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133111399..133111959hg38UCSC Ensembl
Outerchr10:134924903..134925463hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743819, esv2743817
Supporting Variants
SamplesSSM097
Known GenesGPR123
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)essv6891086
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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