A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6955649



Internal ID10064457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:15272380..15272864hg38UCSC Ensembl
Outerchr3:15313887..15314371hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724962
Supporting Variants
SamplesSSM026
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)essv6955649
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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