A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6909258



Internal ID10018205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41559374..41561123hg38UCSC Ensembl
Outerchr15:41851572..41853321hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749609
Supporting Variants
SamplesSSM014
Known GenesTYRO3
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)essv6909258
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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