A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4360



Internal ID15192401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:40380982..40435505hg19UCSC Ensembl
Outerchr19:45072822..45127345hg18UCSC Ensembl
Outerchr19:45072822..45127345hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg1954524
hg1854524
hg1754524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2483
Supporting Variants
SamplesNA12878
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)nssv4360
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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