A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2736274



Internal ID9970606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46270834..46271630hg38UCSC Ensembl
Outerchr10:47642070..47642866hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6734975, essv6861995, essv6752337, essv6819315, essv6856703, essv6965268, essv6672647, essv6763190, essv6976570, essv6958730
SamplesSSM027, SSM087, SSM088, SSM057, SSM029, SSM062, SSM026, SSM031, SSM078, SSM049
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)esv2736274
Frequency
Sample Size96
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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