A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6868190



Internal ID9918166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79346499..79346630hg38UCSC Ensembl
Outerchr18:77106499..77106630hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717637, esv2717636, esv2717497
Supporting Variants
SamplesSSM089
Known GenesATP9B
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)essv6868190
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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