A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6675784



Internal ID10092914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:98126955..98162416hg38UCSC Ensembl
Outerchr3:97845799..97881260hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3835462
hg1935462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2725669
Supporting Variants
SamplesSSM032
Known GenesOR5H1, OR5H14
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)essv6675784
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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