A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6861579



Internal ID9912081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:23549724..23550339hg38UCSC Ensembl
Outerchr8:23407237..23407852hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736758
Supporting Variants
SamplesSSM088
Known GenesSLC25A37
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)essv6861579
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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