A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737760



Internal ID9972099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:141107615..141107855hg38UCSC Ensembl
Outerchr8:142117714..142117954hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6850307, essv6894199, essv6684620, essv6927445, essv6931234, essv6782958, essv6876255, essv6808961, essv6834411
SamplesSSM075, SSM092, SSM019, SSM086, SSM068, SSM082, SSM020, SSM034, SSM012
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)esv2737760
Frequency
Sample Size96
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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