A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4515433



Internal ID7101065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:57169506..57169559hg38UCSC Ensembl
OuterchrX:57169302..57169761hg38UCSC Ensembl
InnerchrX:57195939..57195992hg19UCSC Ensembl
OuterchrX:57195735..57196194hg19UCSC Ensembl
InnerchrX:57212664..57212717hg18UCSC Ensembl
OuterchrX:57212460..57212919hg18UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg38460
hg19460
hg18460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2138770
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)essv4515433
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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