A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2718099



Internal ID9952390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:7688726..7689169hg38UCSC Ensembl
Outerchr19:7753612..7754055hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6895536, essv6921303, essv6874019, essv6666310, essv6696661
SamplesSSM011, SSM017, SSM037, SSM004, SSM098
Known GenesFCER2
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)esv2718099
Frequency
Sample Size96
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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