A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6762227



Internal ID10170704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:153300866..153301590hg38UCSC Ensembl
Outerchr3:153018655..153019379hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2726071
Supporting Variants
SamplesSSM062
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)essv6762227
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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