A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051203



Internal ID21960436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235266465..235266465hg38UCSC Ensembl
chr2:236175109..236175109hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051203
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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