A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5745



Internal ID15196984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:40375507..40429149hg19UCSC Ensembl
Outerchr19:45067347..45120989hg18UCSC Ensembl
Outerchr19:45067347..45120989hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg1953643
hg1853643
hg1753643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2483
Supporting Variants
SamplesNA19129
Known GenesFCGBP
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)nssv5745
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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