A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6763924



Internal ID10170153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:36415065..36427405hg38UCSC Ensembl
Outerchr20:35043468..35055808hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3812341
hg1912341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722375
Supporting Variants
SamplesSSM062
Known GenesDLGAP4
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)essv6763924
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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