A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6686589



Internal ID9756715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:38561695..38562044hg38UCSC Ensembl
Outerchr3:38603186..38603535hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2725164
Supporting Variants
SamplesSSM035
Known GenesSCN5A
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)essv6686589
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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