A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6894422



Internal ID10288461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98407589..98407986hg38UCSC Ensembl
Outerchr10:100167346..100167743hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739973
Supporting Variants
SamplesSSM098
Known GenesPYROXD2
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)essv6894422
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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