A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6732600



Internal ID9796698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:15775257..15775664hg38UCSC Ensembl
Outerchr16:15869114..15869521hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714015, esv2714017
Supporting Variants
SamplesSSM047
Known GenesMYH11
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)essv6732600
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer