A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4773



Internal ID15196495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:106128955..106161512hg38UCSC Ensembl
Outerchr4:107050112..107082669hg19UCSC Ensembl
Outerchr4:107269561..107302118hg18UCSC Ensembl
Outerchr4:107407716..107440273hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3832558
hg1932558
hg1832558
hg1732558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4450
Supporting Variants
SamplesNA19129
Known GenesTBCK
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)nssv4773
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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