A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9865



Internal ID15539938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:31885744..31892649hg38UCSC Ensembl
Outerchr20:30473547..30480452hg19UCSC Ensembl
Outerchr20:29937208..29944113hg18UCSC Ensembl
Outerchr20:29937208..29944113hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3810344
hg1910344
hg1810344
hg1710344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3347
Supporting Variants
SamplesNA18507
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)nssv9865
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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