A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10033



Internal ID15542764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105228317..105247067hg38UCSC Ensembl
Outerchr14:105694654..105713404hg19UCSC Ensembl
Outerchr14:104765699..104784449hg18UCSC Ensembl
Outerchr14:104765699..104784449hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg387515
hg197515
hg187515
hg177515
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1439
Supporting Variants
SamplesNA18956
Known GenesBRF1
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)nssv10033
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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