A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv409



Internal ID15545160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:118182194..118223179hg38UCSC Ensembl
Outerchr4:119103349..119144334hg19UCSC Ensembl
Outerchr4:119322797..119363782hg18UCSC Ensembl
Outerchr4:119460952..119501937hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3840986
hg1940986
hg1840986
hg1740986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4485
Supporting Variants
SamplesNA19240
Known GenesNDST3
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)nssv409
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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