A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6681292



Internal ID9750774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46409104..46410461hg38UCSC Ensembl
Outerchr10:47139290..47140647hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381358
hg191358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736240, esv2736152, esv2736163
Supporting Variants
SamplesSSM033
Known GenesLINC00842
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)essv6681292
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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