A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5548335



Internal ID322102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32300695..32300734hg38UCSC Ensembl
chr21:33673006..33673045hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734691
Samples
Known GenesMRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5548335
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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