A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2729532



Internal ID10313168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:1816453..1817042hg38UCSC Ensembl
Outerchr5:1816567..1817156hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6680142, essv6690178, essv6670661, essv6829901, essv6715244, essv6934394, essv6963233, essv6837168, essv6704750, essv6700727
SamplesSSM036, SSM083, SSM027, SSM039, SSM021, SSM031, SSM033, SSM081, SSM040, SSM043
Known Genes
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)esv2729532
Frequency
Sample Size96
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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