A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5115



Internal ID15549892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:167674906..167720015hg38UCSC Ensembl
Outerchr5:167101911..167147020hg19UCSC Ensembl
Outerchr5:167034489..167079598hg18UCSC Ensembl
Outerchr5:167034489..167079598hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3845110
hg1945110
hg1845110
hg1745110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8187
SamplesNA12156
Known GenesTENM2
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)nsv5115
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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