A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046631



Internal ID21889804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5706086..5706086hg38UCSC Ensembl
chr2:5846218..5846218hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046631
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