A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2224



Internal ID15194821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39850001..39903329hg38UCSC Ensembl
Outerchr19:40340641..40393402hg19UCSC Ensembl
Outerchr19:45032481..45085242hg18UCSC Ensembl
Outerchr19:45032481..45085242hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3853329
hg1952762
hg1852762
hg1752762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2483
Supporting Variants
SamplesNA18555
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)nssv2224
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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