A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2025559



Internal ID7349984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:42087867..42097486hg38UCSC Ensembl
Outerchr12:42087817..42097533hg38UCSC Ensembl
Innerchr12:42481669..42491288hg19UCSC Ensembl
Outerchr12:42481619..42491335hg19UCSC Ensembl
Innerchr12:40767936..40777555hg18UCSC Ensembl
Outerchr12:40767886..40777602hg18UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg389717
hg199717
hg189717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4729907
SamplesNA18507
Known GenesGXYLT1
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)esv2025559
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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