A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056882



Internal ID21966117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143232066..143232066hg38UCSC Ensembl
chr2:143989635..143989635hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529885
Samples
Known GenesARHGAP15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056882
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