A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970



Internal ID15538697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:82732062..82767514hg38UCSC Ensembl
Outerchr11:82443104..82478556hg19UCSC Ensembl
Outerchr11:82120752..82156204hg18UCSC Ensembl
Outerchr11:82120752..82156204hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384296
hg194296
hg184296
hg174296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv413
Supporting Variants
SamplesNA12878
Known GenesFAM181B
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)nssv3970
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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