A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6928790



Internal ID9691309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:28550494..28550725hg38UCSC Ensembl
Outerchr19:29041401..29041632hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718397, esv2718391
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)essv6928790
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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