A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6967530



Internal ID10071782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:49444182..49444233hg38UCSC Ensembl
Outerchr19:49947439..49947490hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718720, esv2718716, esv2718719, esv2718715, esv2718717
Supporting Variants
SamplesSSM027
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)essv6967530
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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