A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757455



Internal ID20533315
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 StatusM
Merged Variants
Supporting Variantsnssv16271735
Samples
Known GenesMFNG
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757455
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