A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154337



Internal ID22084842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36217637..36220823hg38UCSC Ensembl
Outerchr8:36215045..36221919hg38UCSC Ensembl
Innerchr8:36075155..36078341hg19UCSC Ensembl
Outerchr8:36072563..36079437hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386875
hg196875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004403, nssv4004401, nssv4004402, nssv4004407, nssv4004400, nssv4004408, nssv4004405, nssv4004406, nssv4004404
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154337
Frequency
Sample Size131
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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