A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11090



Internal ID15539618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:120208421..120221722hg38UCSC Ensembl
Outerchr4:121129576..121142877hg19UCSC Ensembl
Outerchr4:121349026..121362327hg18UCSC Ensembl
Outerchr4:121487181..121500482hg17UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg389646
hg199646
hg189646
hg179646
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4489
Supporting Variants
SamplesNA15510
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)nssv11090
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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