A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1919320



Internal ID7588624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131709581..131711779hg38UCSC Ensembl
Outerchr7:131709397..131711968hg38UCSC Ensembl
Innerchr7:131394340..131396538hg19UCSC Ensembl
Outerchr7:131394156..131396727hg19UCSC Ensembl
Innerchr7:131044880..131047078hg18UCSC Ensembl
Outerchr7:131044696..131047267hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg382572
hg192572
hg182572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4749501
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)esv1919320
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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