A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4411



Internal ID15202432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86525573..86559362hg38UCSC Ensembl
Outerchr4:87446726..87480515hg19UCSC Ensembl
Outerchr4:87665750..87699539hg18UCSC Ensembl
Outerchr4:87803905..87837694hg17UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg385490
hg195490
hg185490
hg175490
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4760
SamplesNA19129
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)nsv4411
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