A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6739286



Internal ID10150433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:15272326..15272897hg38UCSC Ensembl
Outerchr3:15313833..15314404hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724962
Supporting Variants
SamplesSSM052
Known GenesSH3BP5
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)essv6739286
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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