A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5337



Internal ID15196579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1535551..1540585hg38UCSC Ensembl
Outerchr11:1556781..1561815hg19UCSC Ensembl
Outerchr11:1513357..1518391hg18UCSC Ensembl
Outerchr11:1513357..1518391hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387501
hg197501
hg187501
hg177501
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7640
Supporting Variants
SamplesNA19129
Known GenesMOB2
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)nssv5337
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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