A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6932294



Internal ID10038863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:60816010..60816546hg38UCSC Ensembl
Outerchr15:61108209..61108745hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749758, esv2749756
Supporting Variants
SamplesSSM020
Known GenesRORA
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)essv6932294
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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