A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6699372



Internal ID10110955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1968153..1968322hg38UCSC Ensembl
Outerchr19:1968152..1968321hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717861, esv2717866
Supporting Variants
SamplesSSM038
Known GenesCSNK1G2
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)essv6699372
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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