A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2749900



Internal ID9984184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76006492..76007117hg38UCSC Ensembl
Outerchr15:76298833..76299458hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6846277
SamplesSSM085
Known GenesNRG4
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)esv2749900
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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