A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880



Internal ID15550734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:102864711..102910024hg38UCSC Ensembl
Outerchr7:102505158..102550471hg19UCSC Ensembl
Outerchr7:102292394..102337707hg18UCSC Ensembl
Outerchr7:102099109..102144422hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3845314
hg1945314
hg1845314
hg1745314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564
SamplesNA12878
Known GenesFBXL13
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)nsv5880
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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