A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6672577



Internal ID10090840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6127522..6127635hg38UCSC Ensembl
Outerchr10:6169485..6169598hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731906, esv2731918
Supporting Variants
SamplesSSM031
Known Genes
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)essv6672577
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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