A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6877447



Internal ID9926498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:30462533..30463321hg38UCSC Ensembl
Outerchr19:30953440..30954228hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718441
Supporting Variants
SamplesSSM092
Known GenesZNF536
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)essv6877447
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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