A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156397



Internal ID22086798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:153308618..153312843hg38UCSC Ensembl
Outerchr5:153290424..153313383hg38UCSC Ensembl
Innerchr5:152688178..152692403hg19UCSC Ensembl
Outerchr5:152669984..152692943hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3822960
hg1922960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020347
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156397
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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