A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6695086



Internal ID9761737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:122724728..122750684hg38UCSC Ensembl
Outerchr9:125487007..125512963hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3825957
hg1925957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739015
Supporting Variants
SamplesSSM037
Known GenesOR1L4, OR1L6
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)essv6695086
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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