A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154952



Internal ID22085457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84718257..84806889hg38UCSC Ensembl
Outerchr13:84711720..84813313hg38UCSC Ensembl
Innerchr13:85292392..85381024hg19UCSC Ensembl
Outerchr13:85285855..85387448hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38101594
hg19101594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008271
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154952
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer