A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9593



Internal ID15539721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1575720..1616373hg38UCSC Ensembl
Outerchr20:1556366..1597019hg19UCSC Ensembl
Outerchr20:1504366..1545019hg18UCSC Ensembl
Outerchr20:1504366..1545019hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3840654
hg1940654
hg1840654
hg1740654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3253
Supporting Variants
SamplesNA18507
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)nssv9593
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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