A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2749595



Internal ID9983879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40037607..40037692hg38UCSC Ensembl
Outerchr15:40329808..40329893hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6851837, essv6867662
SamplesSSM089, SSM086
Known GenesSRP14
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)esv2749595
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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