A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2715366



Internal ID10299002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:815097..815885hg38UCSC Ensembl
Outerchr17:718337..719125hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6803940, essv6752998, essv6688798, essv6810966, essv6858168, essv6674195, essv6756016, essv6768979, essv6741583, essv6706771, essv6761396, essv6714665, essv6777533, essv6846428, essv6920874, essv6966821, essv6924951, essv6668514, essv6806840, essv6943984, essv6867933
SamplesSSM008, SSM027, SSM064, SSM087, SSM009, SSM073, SSM074, SSM057, SSM058, SSM018, SSM061, SSM089, SSM017, SSM035, SSM003, SSM031, SSM006, SSM085, SSM040, SSM052, SSM030
Known GenesNXN
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)esv2715366
Frequency
Sample Size96
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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