A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1927



Internal ID15541210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9990812..10022889hg38UCSC Ensembl
Outerchr11:10012359..10044436hg19UCSC Ensembl
Outerchr11:9968935..10001012hg18UCSC Ensembl
Outerchr11:9968935..10001012hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387190
hg197190
hg187190
hg177190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7674
Supporting Variants
SamplesNA18555
Known GenesSBF2
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)nssv1927
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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