A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1933



Internal ID15194530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:46890603..46923886hg38UCSC Ensembl
Outerchr11:46912154..46945437hg19UCSC Ensembl
Outerchr11:46868730..46902013hg18UCSC Ensembl
Outerchr11:46868730..46902013hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg386746
hg196746
hg186746
hg176746
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv310
Supporting Variants
SamplesNA18555
Known GenesLRP4
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)nssv1933
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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