A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6761591



Internal ID10168714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:50300778..50301420hg38UCSC Ensembl
Outerchr20:48917315..48917957hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722497
Supporting Variants
SamplesSSM061
Known GenesLOC284751
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)essv6761591
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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