A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6688026



Internal ID9755222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29169634..29169835hg38UCSC Ensembl
Outerchr10:29458563..29458764hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734883, esv2734606, esv2734894
Supporting Variants
SamplesSSM035
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)essv6688026
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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