A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6826028



Internal ID10226908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183013352..183013460hg38UCSC Ensembl
Outerchr4:183934505..183934613hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2728856, esv2728855
Supporting Variants
SamplesSSM080
Known Genes
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)essv6826028
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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