A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6952558



Internal ID10060843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:18002071..18002898hg38UCSC Ensembl
Outerchr8:17859580..17860407hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736700
Supporting Variants
SamplesSSM025
Known GenesPCM1
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)essv6952558
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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