A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9882



Internal ID15539959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:58363851..58394153hg38UCSC Ensembl
Outerchr5:57659678..57689980hg19UCSC Ensembl
Outerchr5:57695435..57725737hg18UCSC Ensembl
Outerchr5:57695435..57725737hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3830303
hg1930303
hg1830303
hg1730303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4842
Supporting Variants
SamplesNA18507
Known Genes
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)nssv9882
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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