A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075344



Internal ID21984577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155733437..155733437hg38UCSC Ensembl
chr7:155526131..155526131hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571452
Samples
Known GenesRBM33
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075344
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