A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2717402



Internal ID9951692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:76466952..76467674hg38UCSC Ensembl
Outerchr18:74178908..74179630hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6960694, essv6674501, essv6868164, essv6909649, essv6852523, essv6666115, essv6758769, essv6858484, essv6967164, essv6863370, essv6820648
SamplesSSM059, SSM027, SSM087, SSM088, SSM029, SSM026, SSM089, SSM031, SSM014, SSM086, SSM078
Known GenesZNF516
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)esv2717402
Frequency
Sample Size96
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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