A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271735



Internal ID20480953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37484412..37484412hg38UCSC Ensembl
chr22:37880450..37880450hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757455
Supporting Variants
Samples
Known GenesMFNG
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271735
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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