A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10963



Internal ID15192865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:84610311..84641061hg38UCSC Ensembl
Outerchr16:84643917..84674667hg19UCSC Ensembl
Outerchr16:83201418..83232168hg18UCSC Ensembl
Outerchr16:83201418..83232168hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3830751
hg1930751
hg1830751
hg1730751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1911
Supporting Variants
SamplesNA15510
Known GenesCOTL1
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)nssv10963
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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