A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6765575



Internal ID10171754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26603721..26605604hg38UCSC Ensembl
Outerchr10:26892650..26894533hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734384
Supporting Variants
SamplesSSM063
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)essv6765575
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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