A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653624



Internal ID21601929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44954009..44954009hg38UCSC Ensembl
chr13:45528144..45528144hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096403
SamplesNA20509
Known GenesNUFIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653624
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