A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv400



Internal ID15201979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:77943021..77976080hg38UCSC Ensembl
Outerchr11:77654067..77687126hg19UCSC Ensembl
Outerchr11:77331715..77364774hg18UCSC Ensembl
Outerchr11:77331715..77364774hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg386210
hg196210
hg186210
hg176210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5368
SamplesNA19129
Known GenesINTS4
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)nsv400
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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