A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6949388



Internal ID9708172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:77269517..77269973hg38UCSC Ensembl
Outerchr14:77735860..77736316hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2748901
Supporting Variants
SamplesSSM024
Known GenesNGB
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)essv6949388
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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