A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154913



Internal ID22085418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62744411..63055024hg38UCSC Ensembl
Outerchr13:62740311..63062547hg38UCSC Ensembl
Innerchr13:63318544..63629157hg19UCSC Ensembl
Outerchr13:63314444..63636680hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38322237
hg19322237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008145, nssv4008146
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154913
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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