A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9509



Internal ID15539805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105862933..105904795hg38UCSC Ensembl
Outerchr14:106329143..106370653hg19UCSC Ensembl
Outerchr14:105400188..105441698hg18UCSC Ensembl
Outerchr14:105400188..105441698hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3841863
hg1941511
hg1841511
hg1741511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA18507
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)nssv9509
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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