A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6712633



Internal ID10125143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:113174820..113175121hg38UCSC Ensembl
Outerchr9:115937100..115937401hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738953
Supporting Variants
SamplesSSM042
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)essv6712633
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer