A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1583



Internal ID15545491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1578154..1616088hg38UCSC Ensembl
Outerchr20:1558800..1596734hg19UCSC Ensembl
Outerchr20:1506800..1544734hg18UCSC Ensembl
Outerchr20:1506800..1544734hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3837935
hg1937935
hg1837935
hg1737935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3253
Supporting Variants
SamplesNA19240
Known GenesSIRPB1
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)nssv1583
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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