A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6749997



Internal ID10157524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90819050..90819814hg38UCSC Ensembl
Outerchr15:91362280..91363044hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750014
Supporting Variants
SamplesSSM056
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)essv6749997
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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