A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6937367



Internal ID9696155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:49011557..49012134hg38UCSC Ensembl
Outerchr19:49514814..49515391hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718697
Supporting Variants
SamplesSSM021
Known GenesRUVBL2
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)essv6937367
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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