A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5140



Internal ID15549920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:174964921..175009565hg38UCSC Ensembl
Outerchr5:174391924..174436568hg19UCSC Ensembl
Outerchr5:174324530..174369174hg18UCSC Ensembl
Outerchr5:174324530..174369174hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3844645
hg1944645
hg1844645
hg1744645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8201
SamplesNA12156
Known GenesFLJ16171
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)nsv5140
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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