A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4965245



Internal ID7204191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77487587..77487783hg38UCSC Ensembl
Outerchr17:77487435..77487935hg38UCSC Ensembl
Innerchr17:75483669..75483865hg19UCSC Ensembl
Outerchr17:75483517..75484017hg19UCSC Ensembl
Innerchr17:72995264..72995460hg18UCSC Ensembl
Outerchr17:72995112..72995612hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2378475
Supporting Variants
SamplesNA18507
Known GenesSEPT9
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)essv4965245
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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