A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1335



Internal ID15199212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:69569409..69595867hg38UCSC Ensembl
Outerchr14:70036126..70062584hg19UCSC Ensembl
Outerchr14:69105879..69132337hg18UCSC Ensembl
Outerchr14:69105879..69132337hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3826459
hg1926459
hg1826459
hg1726459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2079
SamplesNA18555
Known GenesCCDC177
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv1335
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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