A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154941



Internal ID22085446
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv74n97
Supporting Variantsnssv4008260, nssv4008259
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154941
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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