A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv151



Internal ID15036946
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv151
SamplesNA15510
Known GenesCOTL1
MethodSequencing
AnalysisFosmids were categorized as discordant if the in silico size was in excess of three standard deviations from the mean (<32 or 48> kb) and/or showed incorrect orientation of ends
PlatformCapillary
Comments
ReferenceTuzun_et_al_2005
Pubmed ID15895083
Accession Number(s)nsv151
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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