A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4644



Internal ID15202688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186185600..186219291hg38UCSC Ensembl
Outerchr4:187106754..187140445hg19UCSC Ensembl
Outerchr4:187343748..187377439hg18UCSC Ensembl
Outerchr4:187481903..187515594hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg386341
hg196341
hg186341
hg176341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3143
SamplesNA18555
Known GenesCYP4V2, FLJ38576
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)nsv4644
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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