A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9362



Internal ID15540313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1577327..1615604hg38UCSC Ensembl
Outerchr20:1557973..1596250hg19UCSC Ensembl
Outerchr20:1505973..1544250hg18UCSC Ensembl
Outerchr20:1505973..1544250hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3838278
hg1938278
hg1838278
hg1738278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3253
Supporting Variants
SamplesNA18517
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)nssv9362
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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