A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154953



Internal ID22085458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84813313..84884075hg38UCSC Ensembl
Outerchr13:84806889..84885018hg38UCSC Ensembl
Innerchr13:85387448..85458210hg19UCSC Ensembl
Outerchr13:85381024..85459153hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3878130
hg1978130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008272
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154953
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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