A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv116



Internal ID15383584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76588287..76621947hg38UCSC Ensembl
Outerchr15:76880628..76914288hg19UCSC Ensembl
Outerchr15:74667683..74701343hg18UCSC Ensembl
Outerchr15:74667683..74701343hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3833661
hg1933661
hg1833661
hg1733661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv116
SamplesNA15510
Known GenesSCAPER
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)nsv116
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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