A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6911452



Internal ID9985114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82882886..82888855hg38UCSC Ensembl
Outerchr15:83551638..83557607hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg385970
hg195970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749958
Supporting Variants
SamplesSSM002
Known GenesHOMER2
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)essv6911452
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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