A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10789



Internal ID15195323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1017077..1021900hg38UCSC Ensembl
Outerchr11:1017077..1021900hg19UCSC Ensembl
Outerchr11:1007077..1011900hg18UCSC Ensembl
Outerchr11:1007077..1011900hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3810519
hg1910519
hg1810519
hg1710519
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7637
Supporting Variants
SamplesNA18956
Known GenesMUC6
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)nssv10789
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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