A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5103



Internal ID15549879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:162718093..162745525hg38UCSC Ensembl
Outerchr5:162145099..162172531hg19UCSC Ensembl
Outerchr5:162077677..162105109hg18UCSC Ensembl
Outerchr5:162077677..162105109hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg388390
hg198390
hg188390
hg178390
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2713
SamplesNA18555
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)nsv5103
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