A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2169580



Internal ID7494005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:77252863..77253043hg38UCSC Ensembl
Outerchr18:77252772..77253137hg38UCSC Ensembl
Innerchr18:74964819..74964999hg19UCSC Ensembl
Outerchr18:74964728..74965093hg19UCSC Ensembl
Innerchr18:73093807..73093987hg18UCSC Ensembl
Outerchr18:73093716..73094081hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38366
hg19366
hg18366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4858894
SamplesNA18507
Known GenesGALR1
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)esv2169580
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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