A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11039



Internal ID15539669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:48502430..48519910hg38UCSC Ensembl
Outerchr20:47130676..47136448hg19UCSC Ensembl
Outerchr20:46564083..46569855hg18UCSC Ensembl
Outerchr20:46564083..46569855hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3812106
hg1912106
hg1812106
hg1712106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3406
Supporting Variants
SamplesNA15510
Known Genes
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)nssv11039
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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