A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1645



Internal ID15545422
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 StatusS
Merged Variantsnsv3287
Supporting Variants
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)nssv1645
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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