A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046844



Internal ID21956077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104168506..104168506hg38UCSC Ensembl
chr2:104784964..104784964hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046844
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