A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv432



Internal ID15549017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:92629851..92663633hg38UCSC Ensembl
Outerchr11:92363017..92396799hg19UCSC Ensembl
Outerchr11:92002665..92036447hg18UCSC Ensembl
Outerchr11:92002665..92036447hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg385957
hg195957
hg185957
hg175957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978
SamplesNA12878
Known GenesFAT3
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)nsv432
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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