A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6857933



Internal ID10255623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:100511627..100512003hg38UCSC Ensembl
Outerchr15:101051832..101052208hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750135
Supporting Variants
SamplesSSM087
Known GenesCERS3
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)essv6857933
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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