A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4634494



Internal ID7220126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19977158..19981218hg38UCSC Ensembl
Outerchr16:19976976..19981395hg38UCSC Ensembl
Innerchr16:19988480..19992540hg19UCSC Ensembl
Outerchr16:19988298..19992717hg19UCSC Ensembl
Innerchr16:19895981..19900041hg18UCSC Ensembl
Outerchr16:19895799..19900218hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg384420
hg194420
hg184420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1981290
Supporting Variants
SamplesNA18507
Known Genes
MethodSequencing
AnalysisHierarchical clustering of anomalous readpairs was used to identify groupings of five or more readpairs that had a similar size and position. Read pairs were defined as anomalous if they had high-confidence alignments of each individual read that nevertheless were either incorrectly oriented or implied an insert size of at least 3 standard deviations outside the sample median.
PlatformNot specified
Comments
ReferenceBentley_et_al_2008
Pubmed ID18987734
Accession Number(s)essv4634494
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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