A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6932281



Internal ID9692209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41569033..41570030hg38UCSC Ensembl
Outerchr15:41861231..41862228hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749614
Supporting Variants
SamplesSSM020
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)essv6932281
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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