A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6928758



Internal ID10037966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9112188..9114473hg38UCSC Ensembl
Outerchr19:9222864..9225149hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382286
hg192286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718148
Supporting Variants
SamplesSSM019
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)essv6928758
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer