A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10407



Internal ID15542391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:66972656..67002998hg38UCSC Ensembl
Outerchr4:67838374..67868716hg19UCSC Ensembl
Outerchr4:67520969..67551311hg18UCSC Ensembl
Outerchr4:67667140..67697482hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg389160
hg199160
hg189160
hg179160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4368
Supporting Variants
SamplesNA18956
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)nssv10407
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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