A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1001



Internal ID15544930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:32063202..32087477hg38UCSC Ensembl
Outerchr11:32084748..32109023hg19UCSC Ensembl
Outerchr11:32041324..32065599hg18UCSC Ensembl
Outerchr11:32041324..32065599hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg386794
hg196794
hg186794
hg176794
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7730
Supporting Variants
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)nssv1001
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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