A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7751



Internal ID15552792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:43030496..43064703hg38UCSC Ensembl
Outerchr11:43052046..43086253hg19UCSC Ensembl
Outerchr11:43008622..43042829hg18UCSC Ensembl
Outerchr11:43008622..43042829hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386754
hg196754
hg186754
hg176754
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1006
SamplesNA19240
Known Genes
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)nsv7751
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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