A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019988



Internal ID22081619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11539309..11571638hg38UCSC Ensembl
Outerchr8:11537761..11573481hg38UCSC Ensembl
Innerchr8:11396818..11429147hg19UCSC Ensembl
Outerchr8:11395270..11430990hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3835721
hg1935721
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156837
Supporting Variants
Samples
Known GenesBLK
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019988
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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