A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6692085



Internal ID10105334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:60670570..60670997hg38UCSC Ensembl
Outerchr16:60704474..60704901hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714590
Supporting Variants
SamplesSSM036
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)essv6692085
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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