A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2749769



Internal ID9984053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:62683465..62683624hg38UCSC Ensembl
Outerchr15:62975664..62975823hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6688615, essv6945422
SamplesSSM035, SSM023
Known GenesTLN2
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)esv2749769
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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