A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6862398



Internal ID10010338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:113174825..113175085hg38UCSC Ensembl
Outerchr9:115937105..115937365hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738953
Supporting Variants
SamplesSSM011
Known GenesFKBP15
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)essv6862398
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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