A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6765563



Internal ID10171765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:10938851..10939763hg38UCSC Ensembl
Outerchr10:10980814..10981726hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732884
Supporting Variants
SamplesSSM063
Known GenesLINC00710
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)essv6765563
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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