A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641990



Internal ID21590295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15726132..15726132hg38UCSC Ensembl
chr6:15726363..15726363hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156533
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641990
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