A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6433



Internal ID15537431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1087000..1105164hg38UCSC Ensembl
Outerchr11:1084996..1099072hg19UCSC Ensembl
Outerchr11:1074996..1089072hg18UCSC Ensembl
Outerchr11:1074996..1089072hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388717
hg198717
hg188717
hg178717
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7638
Supporting Variants
SamplesNA12156
Known GenesMUC2
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)nssv6433
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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