A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007068



Internal ID22068699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:18259351..18286194hg38UCSC Ensembl
Outerchr1:18258808..18296689hg38UCSC Ensembl
Innerchr1:18585845..18612688hg19UCSC Ensembl
Outerchr1:18585302..18623183hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3837882
hg1937882
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154655
Supporting Variants
Samples
Known GenesIGSF21
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007068
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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