A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7674



Internal ID15552707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9990812..10029873hg38UCSC Ensembl
Outerchr11:10012359..10051420hg19UCSC Ensembl
Outerchr11:9968935..10007996hg18UCSC Ensembl
Outerchr11:9968935..10007996hg17UCSC 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 StatusM
Merged Variants
Supporting Variantsnssv10801, nssv1927
SamplesNA18956, NA18555
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)nsv7674
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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