A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1919



Internal ID15194516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1517222..1545503hg38UCSC Ensembl
Outerchr11:1538452..1566733hg19UCSC Ensembl
Outerchr11:1495028..1523309hg18UCSC Ensembl
Outerchr11:1495028..1523309hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387422
hg197422
hg187422
hg177422
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7640
Supporting Variants
SamplesNA18555
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)nssv1919
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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