A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561932



Internal ID334898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139726640..139726691hg38UCSC Ensembl
chr4:140647794..140647845hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16958493
Samples
Known GenesMAML3, MGST2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561932
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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