A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6814576



Internal ID10005128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:40117207..40119374hg38UCSC Ensembl
Outerchr19:40623114..40625281hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382168
hg192168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718559
Supporting Variants
SamplesSSM009
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)essv6814576
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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