A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4829171



Internal ID7414803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:135340754..135344006hg38UCSC Ensembl
Outerchr2:135340589..135344168hg38UCSC Ensembl
Innerchr2:136098324..136101576hg19UCSC Ensembl
Outerchr2:136098159..136101738hg19UCSC Ensembl
Innerchr2:135814794..135818046hg18UCSC Ensembl
Outerchr2:135814629..135818208hg18UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg383580
hg193580
hg183580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2058333
Supporting Variants
SamplesNA18507
Known GenesZRANB3
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)essv4829171
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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