A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6958733



Internal ID9720545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46295462..46295614hg38UCSC Ensembl
Outerchr10:47666698..47666850hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736351, esv2736163, esv2736363
Supporting Variants
SamplesSSM026
Known GenesANTXRL
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)essv6958733
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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