A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6729168



Internal ID10139732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:14044586..14044734hg38UCSC Ensembl
Outerchr20:14025232..14025380hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722204
Supporting Variants
SamplesSSM046
Known GenesMACROD2
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)essv6729168
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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