A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6810802



Internal ID10213767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:171502716..171503228hg38UCSC Ensembl
Outerchr3:171220505..171221017hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2726201
Supporting Variants
SamplesSSM076
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)essv6810802
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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