A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11082



Internal ID15539626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:35584762..35615458hg38UCSC Ensembl
Outerchr4:35586384..35617080hg19UCSC Ensembl
Outerchr4:35262779..35293475hg18UCSC Ensembl
Outerchr4:35408950..35439646hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg389152
hg199152
hg189152
hg179152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4297
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)nssv11082
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer