A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154922



Internal ID22085427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64726321..64740963hg38UCSC Ensembl
Outerchr13:64708530..64745216hg38UCSC Ensembl
Innerchr13:65300453..65315095hg19UCSC Ensembl
Outerchr13:65282662..65319348hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3836687
hg1936687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008160, nssv4008158, nssv4008159
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154922
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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