A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6921



Internal ID15190257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1446758..1479317hg38UCSC Ensembl
Outerchr20:1427403..1459962hg19UCSC Ensembl
Outerchr20:1375403..1407962hg18UCSC Ensembl
Outerchr20:1375403..1407962hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386882
hg196882
hg186882
hg176882
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3252
Supporting Variants
SamplesNA12156
Known GenesNSFL1C, SIRPB2
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)nssv6921
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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