A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008146



Internal ID22069777
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154913
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008146
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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