A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154948



Internal ID22085453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83960215..84065501hg38UCSC Ensembl
Outerchr13:83958142..84069021hg38UCSC Ensembl
Innerchr13:84534350..84639636hg19UCSC Ensembl
Outerchr13:84532277..84643156hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38110880
hg19110880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008268
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154948
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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