A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626771



Internal ID21575076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186433255..186433255hg38UCSC Ensembl
chr4:187354409..187354409hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120841
SamplesNA18534
Known GenesF11-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626771
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