A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1942



Internal ID15541225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63429088..63450487hg38UCSC Ensembl
Outerchr11:63196560..63217959hg19UCSC Ensembl
Outerchr11:62953136..62974535hg18UCSC Ensembl
Outerchr11:62953136..62974535hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3816182
hg1916182
hg1816182
hg1716182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv351
Supporting Variants
SamplesNA18555
Known GenesMIR3680-1, MIR3680-2
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)nssv1942
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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