A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154901



Internal ID22085406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:56479678..56588432hg38UCSC Ensembl
Outerchr13:56475381..56591671hg38UCSC Ensembl
Innerchr13:57053812..57162566hg19UCSC Ensembl
Outerchr13:57049515..57165805hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38116291
hg19116291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008108
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154901
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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