A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6965451



Internal ID10069658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133111265..133111765hg38UCSC Ensembl
Outerchr10:134924769..134925269hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743819, esv2743818, esv2743817
Supporting Variants
SamplesSSM027
Known GenesGPR123
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)essv6965451
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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