A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154969



Internal ID22085474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101018947..101021691hg38UCSC Ensembl
Outerchr13:101017799..101024844hg38UCSC Ensembl
Innerchr13:101671299..101674043hg19UCSC Ensembl
Outerchr13:101670151..101677196hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg387046
hg197046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008301
Samples
Known GenesNALCN-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154969
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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