A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6960919



Internal ID9716483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:2805868..2806018hg38UCSC Ensembl
Outerchr19:2805866..2806016hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717912, esv2717913
Supporting Variants
SamplesSSM026
Known GenesTHOP1
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)essv6960919
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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