A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647241



Internal ID21839288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39956636..39956636hg38UCSC Ensembl
chr22:40352640..40352640hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108428
Supporting Variants
Samples
Known GenesGRAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647241
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