A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008260



Internal ID22069891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76713294..76726079hg38UCSC Ensembl
Outerchr13:76710653..76726342hg38UCSC Ensembl
Innerchr13:77287429..77300214hg19UCSC Ensembl
Outerchr13:77284788..77300477hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3815690
hg1915690
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154941
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008260
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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