A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10291



Internal ID15542507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:31871679..31901524hg38UCSC Ensembl
Outerchr20:30459482..30489327hg19UCSC Ensembl
Outerchr20:29923143..29952988hg18UCSC Ensembl
Outerchr20:29923143..29952988hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg389665
hg199665
hg189665
hg179665
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3347
Supporting Variants
SamplesNA18956
Known GenesTTLL9
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)nssv10291
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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