A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6932994



Internal ID9694619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:49875124..49875586hg38UCSC Ensembl
Outerchr19:50378381..50378843hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718725, esv2718724
Supporting Variants
SamplesSSM020
Known GenesAKT1S1
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)essv6932994
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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