A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4558905



Internal ID7144537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15465105..15465295hg38UCSC Ensembl
Outerchr17:15464898..15465512hg38UCSC Ensembl
Innerchr17:15368419..15368609hg19UCSC Ensembl
Outerchr17:15368212..15368826hg19UCSC Ensembl
Innerchr17:15309144..15309334hg18UCSC Ensembl
Outerchr17:15308937..15309551hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38615
hg19615
hg18615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2346287
Supporting Variants
SamplesNA18507
Known GenesCDRT4, TVP23C-CDRT4
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)essv4558905
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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