A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6917965



Internal ID9681759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:10018605..10019053hg38UCSC Ensembl
Outerchr3:10060289..10060737hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724893, esv2724891, esv2724892
Supporting Variants
SamplesSSM017
Known GenesCIDECP
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)essv6917965
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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