A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156837



Internal ID22087238
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019988
Samples
Known GenesBLK
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156837
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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