A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9863



Internal ID15539936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:13945594..13962726hg38UCSC Ensembl
Outerchr20:13926240..13943372hg19UCSC Ensembl
Outerchr20:13874240..13891372hg18UCSC Ensembl
Outerchr20:13874240..13891372hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg386619
hg196619
hg186619
hg176619
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3296
Supporting Variants
SamplesNA18507
Known GenesSEL1L2
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)nssv9863
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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