A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6907190



Internal ID9673381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:1206298..1206382hg38UCSC Ensembl
Outerchr5:1206413..1206497hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729441, esv2729442
Supporting Variants
SamplesSSM014
Known GenesSLC6A19
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)essv6907190
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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