A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6763755



Internal ID9823314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89648680..89648956hg38UCSC Ensembl
Outerchr16:89715088..89715364hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2715190
Supporting Variants
SamplesSSM062
Known GenesCHMP1A
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)essv6763755
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