A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4550335



Internal ID7135967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8343307..8344741hg38UCSC Ensembl
Outerchr17:8343216..8344844hg38UCSC Ensembl
Innerchr17:8246625..8248059hg19UCSC Ensembl
Outerchr17:8246534..8248162hg19UCSC Ensembl
Innerchr17:8187350..8188784hg18UCSC Ensembl
Outerchr17:8187259..8188887hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381629
hg191629
hg181629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1978259
Supporting Variants
SamplesNA18507
Known GenesODF4
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)essv4550335
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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