A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651580



Internal ID21599885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29556165..29556165hg38UCSC Ensembl
chr11:29577712..29577712hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074174
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651580
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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