A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3287



Internal ID15547881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161994001..162027363hg38UCSC Ensembl
Outerchr1:161963791..161997153hg19UCSC Ensembl
Outerchr1:160230415..160263777hg18UCSC Ensembl
Outerchr1:158695449..158728811hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387628
hg197628
hg187628
hg177628
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1645
SamplesNA19240
Known GenesOLFML2B
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)nsv3287
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