A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6886766



Internal ID10281749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:628301..628953hg38UCSC Ensembl
Outerchr5:628416..629068hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729333
Supporting Variants
SamplesSSM096
Known GenesCEP72
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)essv6886766
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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